2024 Cell signaling tech - Monoclonal Antibody for studying H3 (Ser10) phosphate. Cited in 454 publications. Validated for WB, IF, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, Phospho-Histone H3 (Ser10) (6G3) Mouse Monoclonal Antibody (CST #9706) is …

 
 For reproducible data, Cell Signaling Technology (CST) offers rigorously validated and reliable products including antibodies, reagents, and kits for biological research. We have a substantial portfolio of products to interrogate mechanisms of cellular health and disease. Whether in the fields of cancer, immunology, infectious disease ... . Cell signaling tech

Species Cross-Reactivity Key: Polyclonal Antibody for studying eNOS. Cited in 167 publications. Validated for Western Blotting. Highly specific and rigorously validated in-house, eNOS Antibody (CST #9572) is ready to ship.Application Key: WB-Western IP-Immunoprecipitation IHC-Immunohistochemistry ChIP-Chromatin Immunoprecipitation IF-Immunofluorescence F-Flow Cytometry Species Cross-Reactivity Key: H-Human M-Mouse R-Rat Hm-Hamster Mk-Monkey Vir-Virus Mi-Mink C-Chicken Dm-D. melanogaster X-Xenopus Z-Zebrafish B-Bovine Dg-Dog Pg-Pig Sc-S. cerevisiae Ce-C. … Western blot analysis was performed using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb. Anti-rabbit IgG, HRP-linked Antibody #7074 was used as a secondary antibody. Confocal immunofluorescent analysis of HeLa cells, serum starved (left) or TNF-α treated (#8902 at 20 ng/ml for 20 min, right), using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb ... Phospho-Akt substrate-specific antibodies from Cell Signaling Technology are powerful tools for investigating the regulation of phosphorylation by Akt and other Arg-directed kinases, as well as for high throughput kinase drug discovery. Montminy, M. (1997) Annu Rev Biochem 66, 807-22. Pearson, R.B. and Kemp, B.E. (1991) Methods Enzymol 200, …Specificity / Sensitivity. Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb detects endogenous levels of 4E-BP1 only when phosphorylated at Thr37 and/or Thr46. This antibody may cross-react with 4E-BP2 and 4E-BP3 when phosphorylated at equivalent sites. Non-specific staining has been observed in mitotic cells by immunofluorescence.Background. TAK1 is a mitogen-activated protein kinase kinase kinase that can be activated by TGF-β, bone morphogenetic protein and other cytokines including IL-1 (1,2). In vivo activation of TAK1 requires association with TAK1 binding protein 1 (TAB1), which triggers phosphorylation of TAK1 (3,4).This is true whether the cell is a single-celled organism or part of a larger, more complex multicellular organism. Cells communicate with their environment through a process called signaling. Cell signaling is how the cell collects information and then responds with an action at the correct time. Signaling is the initial event associated with ... Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody. For a carrier free (BSA and azide free) version of this product see product # 63411. Western blot analysis was performed using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb. Anti-rabbit IgG, HRP-linked Antibody #7074 was used as a secondary antibody. Confocal immunofluorescent analysis of HeLa cells, serum starved (left) or TNF-α treated (#8902 at 20 ng/ml for 20 min, right), using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb ... The c-Myc Antibody confirms silencing of c-Myc expression, and the p42 MAPK Antibody is used to control for protein loading and siRNA specificity. Western blot analysis of extracts from HeLa, BaF3 and NBT-11 cells, using c-Myc Antibody. Simple Western™ analysis of lysates (1 mg/mL) from HeLa cells using c-Myc Antibody #9402.Pin1 is a small (18 kDa) protein with two distinct functional domains: an amino-terminal WW domain and a carboxy-terminal PPlase domain. Pin1 interacts with several mitotic phosphoproteins, including Plk1, cdc25C and cdc27, and is thought to act as a phosphorylation-dependent PPlase for these target molecules (7-9).Specificity and sensitivity of Phospho-p44/42 MAPK (Erk1/2) (Thr202/Tyr204) Antibody. The antibody reacts specifically with as little as 0.25 ng of phosphorylated p42 MAP kinase and does not cross-react with up to 4 µg of nonphosphorylated p42 MAP kinase. Western blot analysis of whole-cell extracts from unstarved wild-type mouse embryonic ... For reproducible data, Cell Signaling Technology (CST) offers rigorously validated and reliable products including antibodies, reagents, and kits for biological research. We have a substantial portfolio of products to interrogate mechanisms of cellular health and disease. Whether in the fields of cancer, immunology, infectious disease ... Immunohistochemistry (IHC) staining allows for 2 broad classes of detection: 1) chromogenic and 2) fluorescent. For chromogenic detection, CST recommends using polymer-based systems that avoid the limitations of the biotin-based system while also increasing sensitivity of the assay. Try SignalStain ® Boost IHC Detection Reagent (HRP, …p70 S6 kinase is a mitogen activated Ser/Thr protein kinase that is required for cell growth and G1 cell cycle progression (1,2). p70 S6 kinase phosphorylates the S6 protein of the 40S ribosomal subunit and is involved in translational control of 5' oligopyrimidine tract mRNAs (1). A second isoform, p85 S6 kinase, is derived from the same gene ...Simple Western™ analysis of lysates (0.1 mg/mL) from COS-7 cells, transfected with a construct expressing HA-tagged Stat3 using HA-Tag (6E2) Mouse mAb #2367. The virtual lane view (left) shows a single target band (as indicated) at 1:50 and 1:250 dilutions of primary antibody.Lanes 1 & 2 are 5% input. Confocal immunofluorescent analysis of NCI-H1299 cells, untreated (left) or λ-phosphatase-treated (right), using Phospho-DRP1 (Ser616) Antibody (green). Actin filaments have been labeled with DY-554 phallodin (red). Blue pseudocolor = DRAQ5 ® (fluorescent DNA dye).DIVERSITY, EQUITY, & INCLUSION. CST understands the importance of a safe and diverse workplace. Different perspectives and ideas drive collaboration and innovation. By providing an inclusive and stimulating work environment, we aim to establish human dignity and meaningful work as an essential part of our culture. Embrace the. culture.Flow cytometric analysis of HeLa (blue) and Karpas620 cells (green) using Blimp-1/PRDI-BF1 (C14A4) Rabbit mAb (solid lines) or a concentration-matched Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900 (dashed lines). Anti-rabbit IgG (H+L), F (ab') 2 Fragment (Alexa Fluor ® 488 Conjugate) #4412 was used as a secondary antibody. Western blot ... Incubate membrane with Anti-mouse IgG, HRP-linked Antibody ( #7076 at 1:2000) and Anti-biotin, HRP-linked Antibody ( #7075 at 1:1000–1:3000) to detect biotinylated protein markers in 10 ml of blocking buffer with gentle agitation for 1 hr at room temperature. Wash three times for 5 min each with 15 ml of TBST. Proceed with detection (Section D). In smooth muscle, MLC2 is phosphorylated at Thr18 and Ser19 by myosin light chain kinase (MLCK) in a Ca 2+ /calmodulin-dependent manner (1). This phosphorylation is correlated with myosin ATPase activity and smooth muscle contraction (2). ROCK also phosphorylates Ser19 of smooth muscle MLC2, which regulates the assembly of stress fibers (3).Apr 15, 2022 · Cell Signaling Technology (CST) emphasizes that it was founded by scientists, for scientists. This is at the core of the company’s culture and permeates all its decisions. Headed by neuroscientist Michael Comb, CST seeks to deeply understand the requirements of their customers—bench researchers who are in the weeds of complex research ... Checking the Cell Signaling Technology ® (CST ®) website, you are in luck! There are mouse reactive flow-validated antibody conjugates available against each target: CD4 …Flow cytometric analysis of HeLa (blue) and Karpas620 cells (green) using Blimp-1/PRDI-BF1 (C14A4) Rabbit mAb (solid lines) or a concentration-matched Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900 (dashed lines). Anti-rabbit IgG (H+L), F (ab') 2 Fragment (Alexa Fluor ® 488 Conjugate) #4412 was used as a secondary antibody. Western blot ...Cell Signaling Technology has an overall rating of 4.5 out of 5, based on over 132 reviews left anonymously by employees. 96% of employees would recommend working at Cell Signaling Technology to a friend and 96% have a positive outlook for the business. This rating has improved by 2% over the last 12 months.Polyclonal Antibody for studying Flag-Tag. Cited in 774 publications. Validated for WB, IP, F. Available in 2 sizes. Highly specific and rigorously validated in-house, DYKDDDDK Tag Antibody (Binds to same epitope as Sigma-Aldrich Anti-FLAG M2 antibody) (CST #2368) is …Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min.If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.Science & Development. As a company of scientists for scientists, we are passionate about the discovery and development of innovative therapies for human disease. Help advance …Product Description. Designed for use with rabbit polyclonal and monoclonal antibodies, this affinity purified goat anti-rabbit IgG (heavy and light chain) antibody is conjugated to horseradish peroxidase (HRP) for chemiluminescent detection. This product is thoroughly validated with CST primary antibodies and will work optimally with the CST ...Western blot analysis of extracts from various cell lines using GAPDH (14C10) Rabbit mAb. Simple Western™ analysis of lysates (0.01 mg/mL) from HeLa cells using GAPDH (14C10) Rabbit mAb #2118. The virtual lane view (left) shows a single target band (as indicated) at 1:10 and 1:50 dilutions of primary antibody.If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.Western blot analysis of extracts from various cell lines using GAPDH (D16H11) XP ® Rabbit mAb. Simple Western™ analysis of lysates (0.1 mg/mL) from HeLa cells using GAPDH (D16H11) XP ® Rabbit mAb #5174. The virtual lane view (left) shows a single target band (as indicated) at 1:10 and 1:50 dilutions of primary antibody.Monoclonal Antibody for studying LC3B. Cited in 138 publications. Validated for WB, IP, IHC, IF, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, LC3B (E5Q2K) Mouse Monoclonal Antibody (CST #83506) is ready to ship.Mar 14, 2023 · A complete, step-by-step walkthrough of the CUT&RUN Protocol included with the CUT&RUN Assay kit (#86652) from Cell Signaling Technology (CST). • Visit the ... The Harper Lab studies mechanisms underlying cellular homeostasis and signaling, with a focus on the ubiquitin system and the autophagy-lysosome system. The interest in the …Western blot analysis of extracts from various cell lines using GAPDH (14C10) Rabbit mAb. Simple Western™ analysis of lysates (0.01 mg/mL) from HeLa cells using GAPDH (14C10) Rabbit mAb #2118. The virtual lane view (left) shows a single target band (as indicated) at 1:10 and 1:50 dilutions of primary antibody.Species Cross-Reactivity Key: Polyclonal Antibody for studying DRP1 (Ser616) phosphate. Cited in 343 publications. Validated for WB, IP, IF, F. Highly specific and rigorously validated in-house, Phospho-DRP1 (Ser616) Antibody (CST #3455) is ready to ship.Cell signaling is a fundamental property of all cellular life in prokaryotes and eukaryotes . Typically, the signaling process involves three components: the signal, the receptor, and the effector. [citation needed] In biology, signals are mostly chemical in nature, but can also be physical cues such as pressure, voltage, temperature, or light.Immunoprecipitation of Bax from HepG2 cells. Lane 1 is 10% input, lane 2 is precipitated with Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900, and lane 3 is Bax (D2E11) Rabbit mAb, #5023. Western blot was performed …Immunoprecipitation of TIM-3 from RPMI 8226 cell extracts. Lane 1 is 10% input, lane 2 is precipitated with Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900, and lane 3 is TIM-3 (D5D5R ™) XP ® Rabbit mAb, #45208. Western blot was performed using TIM-3 (D5D5R ™) XP ® Rabbit mAb.Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min.If you're looking for a career that you can feel good about with a company that cares about you, the environment, and our communities, look no further than Cell Signaling Technology. Check out our current career …Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min.Prepare 1X SignalFire™ ECL Reagent ( #6883) by diluting one part 2X Reagent A and one part 2X Reagent B (e.g. for 10 ml, add 5 ml Reagent A and 5 ml Reagent B). Mix well. Incubate substrate with membrane for 1 minute, remove excess solution (membrane remains wet), wrap in plastic and expose to X-ray film. Learn & Support. Use this Directory to navigate to a wealth of informative resources about molecular targets and the protocols and tools needed to study them efficiently. Under "Education & Resources" you will find links to a large collection of educational resources, including our PhosphoSitePlus® PTM Database, useful reference tables, guides ... The absence of signal in the HCT 116 knockout cells confirms the specificity of the antibody for LC3B. Western blot analysis of extracts from HeLa, C2C12, and KNRK cells, untreated (-) or treated with Chloroquine (50 μM, overnight; +) #14774 using LC3B (E5Q2K) Mouse mAb (upper) or β-Actin (D6A8) Rabbit mAb #8457 (lower).Solutions for Neurodegeneration Drug Discovery. Download “Solutions for Advancing Neurodenerative Therapeutics Discovery” and discover more! An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for …If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.Cell Signaling Technology (CST) a private company founded by scientist, understands your need to make decision with confidence, providing the best-in-class products and services. No vendor is more stringent about antibody validation than CST, so when you partner with us you get results you can trust faster, to move your oncology project forward ...If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.Lane 1 is 10% input, lane 2 is USP18 (D4E7) Rabbit mAb, and lane 3 is Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900. Western blot analysis was perfomed using USP18 (D4E7) Rabbit mAb. Anti-rabbit IgG, HRP-linked Antibody #7074 was used as a secondary antibody. To Purchase # 4813. Cat.Cell Signaling Technology has an overall rating of 4.5 out of 5, based on over 132 reviews left anonymously by employees. 96% of employees would recommend working at Cell Signaling Technology to a friend and 96% have a positive outlook for the business. This rating has improved by 2% over the last 12 months.Cell Signaling Technology (CST) is a different kind of life sciences company—one founded, owned, and run by active research scientists, with the highest standards …Prepare 1X SignalFire™ ECL Reagent ( #6883) by diluting one part 2X Reagent A and one part 2X Reagent B (e.g. for 10 ml, add 5 ml Reagent A and 5 ml Reagent B). Mix well. Incubate substrate with membrane for 1 minute, remove excess solution (membrane remains wet), wrap in plastic and expose to X-ray film.Specificity / Sensitivity. Phospho-4E-BP1 (Thr37/46) (236B4) Rabbit mAb detects endogenous levels of 4E-BP1 only when phosphorylated at Thr37 and/or Thr46. This antibody may cross-react with 4E-BP2 and 4E-BP3 when phosphorylated at equivalent sites. Non-specific staining has been observed in mitotic cells by immunofluorescence.PARP, a 116 kDa nuclear poly (ADP-ribose) polymerase, appears to be involved in DNA repair in response to environmental stress (1). This protein can be cleaved by many ICE-like caspases in vitro (2,3) and is one of the main cleavage targets of caspase-3 in vivo (4,5). In human PARP, the cleavage occurs between Asp214 and Gly215, which separates ...Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min.DIVERSITY, EQUITY, & INCLUSION. CST understands the importance of a safe and diverse workplace. Different perspectives and ideas drive collaboration and innovation. By providing an inclusive and stimulating work environment, we aim to establish human dignity and meaningful work as an essential part of our culture. Embrace the. culture.Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min.Polyclonal Antibody for studying Flag-Tag. Cited in 774 publications. Validated for WB, IP, F. Available in 2 sizes. Highly specific and rigorously validated in-house, DYKDDDDK Tag Antibody (Binds to same epitope as Sigma-Aldrich Anti-FLAG M2 antibody) (CST #2368) is …Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min.Monoclonal Antibody for studying LC3B. Cited in 138 publications. Validated for WB, IP, IHC, IF, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, LC3B (E5Q2K) Mouse Monoclonal Antibody (CST #83506) is ready to ship. GPX4 converts lipid hydroperoxides to non-toxic lipid alcohols, therefore preventing ferroptosis (2). Research studies show that selenium enhances GPX4 expression and inhibits ferroptotic death to protect neurons (3). In addition, some therapy-resistant cancer cells depend on GPX4 to survive. About Cell Signaling Technology Cell Signaling Technology (CST) is a different kind of life sciences company—one founded, owned, and run by active research scientists, with the highest standards of product and service quality, technological innovation, and scientific rigor. Founded in 1999 and headquartered in Danvers, …Monoclonal Antibody for studying Flag-Tag. Cited in 478 publications. Validated for WB, IP, IHC, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, DYKDDDDK Tag (9A3) Mouse Monoclonal Antibody (Binds to same epitope as Sigma-Aldrich Anti-FLAG M2 antibody) (CST #8146) is ready to ship. 抗体不应成为您实验中的变量之一。了解客户为何在抗体特异性和敏感性方面给予 cst 最高评价。 Monoclonal Antibody for studying EEA1. Cited in 345 publications. Validated for WB, IP, IF, IF. Available in 2 sizes. Highly specific and rigorously validated in-house, EEA1 (C45B10) Rabbit Monoclonal Antibody (CST #3288) is ready to ship. Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min.If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.Poster: Signaling Pathways | Cell Signaling Technology. This poster provides a comprehensive overview of the major signaling pathways involved in cell growth, survival, differentiation, and stress responses. Download the PDF to explore the key molecules and interactions that regulate these pathways and their implications for human health and …Western blot analysis of extracts from various cell lines using GAPDH (14C10) Rabbit mAb. Simple Western™ analysis of lysates (0.01 mg/mL) from HeLa cells using GAPDH (14C10) Rabbit mAb #2118. The virtual lane view (left) shows a single target band (as indicated) at 1:10 and 1:50 dilutions of primary antibody.Partnerships & Licensing. As a trusted partner, CST is focused on building symbiotic relationships to maximize the value of products, technology, and intellectual property; whether ours or our partner’s. True innovation is collaborative. We have broad interest in technology licensing, scientific and technical collaborations, and commercial ... Contact Technical Support. Hours: 8:00 AM - 6:00 PM (EST) Phone: 877-678-8324. Email: [email protected]. Polyclonal Antibody for studying H3 (Ser10) phosphate. Cited in 1110 publications. Validated for WB, IHC, IF. Available in 2 sizes. Highly specific and rigorously validated in-house, Phospho-Histone H3 (Ser10) Antibody (CST #9701) is ready to ship. For reproducible data, Cell Signaling Technology (CST) offers rigorously validated and reliable products including antibodies, reagents, and kits for biological research. We have a substantial portfolio of products to interrogate mechanisms of cellular health and disease. Whether in the fields of cancer, immunology, infectious disease ... Monoclonal Antibody for studying LC3B. Cited in 138 publications. Validated for WB, IP, IHC, IF, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, LC3B (E5Q2K) Mouse Monoclonal Antibody (CST #83506) is ready to ship.Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody. Cathepsin B (D1C7Y) XP ® Rabbit mAb recognizes endogenous levels of total cathepsin B protein.Species Cross-Reactivity Key: Polyclonal Antibody for studying DRP1 (Ser616) phosphate. Cited in 343 publications. Validated for WB, IP, IF, F. Highly specific and rigorously validated in-house, Phospho-DRP1 (Ser616) Antibody (CST #3455) is ready to ship. CD31 (Platelet Endothelial Cell Adhesion Molecule-1: PECAM-1), a member of the Ig superfamily of cell adhesion molecules, is expressed by circulating platelets, monocytes, neutrophils, some T cells, and endothelial cells and modulates cell adhesion, endothelial cell migration, and angiogenesis (1). CD31 is phosphorylated on Tyr686 at the ... Immunohistochemistry (IHC) staining allows for 2 broad classes of detection: 1) chromogenic and 2) fluorescent. For chromogenic detection, CST recommends using polymer-based systems that avoid the limitations of the biotin-based system while also increasing sensitivity of the assay. Try SignalStain ® Boost IHC Detection Reagent (HRP, …Cell Signaling Technology (CST) is dedicated to providing the world’s highest quality, innovative research products to accelerate biological understanding. A privately …Cell Signaling Technology is a private, family-owned company that operates in the field of applied systems biology research, particularly focusing on cancer. The company's main offerings include the development and production of antibodies, which are validated for multiple applications by their team of Ph.D. level scientists.Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C.NOTE: Most antibodies from Cell Signaling Technology work optimally between 1 and 2 ug per IP sample. In the case where there are multiple samples with varying concentrations, …Target duluth, Hmd trucking, Nook and cranny, 102.1 magic, Tulsa bone and joint tulsa ok, Pacific garden mission chicago, Villa nova stickney, Walmart temple, Olive garden augusta ga, Pinnacle eye group, Aandr bbq, Temple san francisco, American first finance phone number, Cattle country fest

Learn & Support. Use this Directory to navigate to a wealth of informative resources about molecular targets and the protocols and tools needed to study them efficiently. Under "Education & Resources" you will find links to a large collection of educational resources, including our PhosphoSitePlus® PTM Database, useful reference tables, guides ... . Resound internet

cell signaling techameriair

The LC3B (D11) XP ® Rabbit mAb confirms silencing of LC3B expression, while the α-Tubulin (11H10) Rabbit mAb is used to control for loading and specificity of LC3B siRNA. Show More. Simple Western™ analysis of lysates (1mg/ml) from HeLa cells treated with Chloroquine (50uM, O/N) using LC3B (D11) XP ® Rabbit mAb #3868.Cell Signaling Technology (CST) | 21,261 followers on LinkedIn. CST is a private, family-owned company, founded by scientists and dedicated to providing high-quality research tools. | Founded by ...If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.The biological functions of HSP70/HSP90 extend beyond their chaperone activity. They are essential for the maturation and inactivation of nuclear hormones and other signaling molecules (1,3). They also play a role in vesicle formation and protein trafficking (2). Nollen, E.A. and Morimoto, R.I. (2002) J. Cell Sci. 115, 2809-2816.Use the Cell Signaling Technology Technical Documentation search tool to find Product Data Sheets, Certificates of Analysis (CoA), and Safety Data Sheets (SDS). Begin your search by entering the product number in the search field. Online publication of this documentation makes it easier for you to access it, and more environmentally friendly ... ELISA: An Introduction. Enzyme-linked immunosorbent assay (ELISA) allows for the quantification of a molecule of interest using antibodies and tags (such as the enzyme horseradish peroxidase [HRP]), either directly or indirectly coupled to the antibody for detection. ELISA can be used with a variety of sample types, such as cell lysate, tissue ... In smooth muscle, MLC2 is phosphorylated at Thr18 and Ser19 by myosin light chain kinase (MLCK) in a Ca 2+ /calmodulin-dependent manner (1). This phosphorylation is correlated with myosin ATPase activity and smooth muscle contraction (2). ROCK also phosphorylates Ser19 of smooth muscle MLC2, which regulates the assembly of stress fibers (3).Rab -Rabbit. All -All Species Expected. Polyclonal Antibody for studying H2AX (Ser139) phosphate. Cited in 1048 publications. Validated for WB, WB, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, Phospho-Histone H2A.X (Ser139) Antibody (CST #2577) is ready to ship.Cell Signaling Technology (CST) is a different kind of life sciences company—one founded, owned, and run by active research scientists, with the highest standards of product and service quality ...Solutions for Neurodegeneration Drug Discovery. Download “Solutions for Advancing Neurodenerative Therapeutics Discovery” and discover more! An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for …Science & Development. As a company of scientists for scientists, we are passionate about the discovery and development of innovative therapies for human disease. Help advance … The p53 tumor suppressor protein plays a major role in cellular response to DNA damage and other genomic aberrations. Activation of p53 can lead to either cell cycle arrest and DNA repair or apoptosis (1). p53 is phosphorylated at multiple sites in vivo and by several different protein kinases in vitro (2,3). Vascular endothelial growth factor receptor 2 (VEGFR2, KDR, Flk-1) is a major receptor for VEGF-induced signaling in endothelial cells. Upon ligand binding, VEGFR2 undergoes autophosphorylation and becomes activated (1). Major autophosphorylation sites of VEGFR2 are located in the kinase insert domain (Tyr951/996) and in the tyrosine kinase ...Species Cross-Reactivity Key: Polyclonal Antibody for studying eNOS. Cited in 167 publications. Validated for Western Blotting. Highly specific and rigorously validated in-house, eNOS Antibody (CST #9572) is ready to ship.Cell signaling is a fundamental property of all cellular life in prokaryotes and eukaryotes . Typically, the signaling process involves three components: the signal, the receptor, and the effector. [citation needed] In biology, signals are mostly chemical in nature, but can also be physical cues such as pressure, voltage, temperature, or light.The innate immune system mainly consists of phagocytic cells, such as neutrophils, macrophages, natural killer cells, basophils, and others that target dangerous invading organisms. The cells of the adaptive immune system are T cells and B cells. Natural killer (NK) T cells have features of both innate and adaptive immune cells.The matrix metalloproteinases (MMPs) are a family of proteases that target many extracellular proteins including other proteases, growth factors, cell surface receptors, and adhesion molecules (1). Among the family members, MMP-2, MMP-3, MMP-7, and MMP-9 have been characterized as important factors for normal tissue remodeling during embryonic ...Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody. For a carrier free (BSA and azide free) version of this product see product # 63411.Ferroptosis is an iron-dependent form of regulated cell death associated with an increase in lipid peroxides (reviewed in 1,2). Free divalent iron (Fe2+) can lead to spontaneous lipid peroxidation through a Fenton reaction. Ferroptosis is regulated by signaling pathways that control iron storage and oxidative stress.If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation. Lane 1 is 10% input, lane 2 is Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900, and lane 3 is β3-Tubulin (D71G9) XP ® Rabbit mAb. Western blot analysis was performed using β3-Tubulin (D71G9) XP ® Rabbit mAb. Mouse Anti-rabbit IgG (Conformation Specific) (L27A9) mAb #3678 was used as the secondary antibody. Use the Cell Signaling Technology Technical Documentation search tool to find Product Data Sheets, Certificates of Analysis (CoA), and Safety Data Sheets (SDS). Begin your search by entering the product number in the search field. Online publication of this documentation makes it easier for you to access it, and more environmentally friendly ...NKX2.5 plays an essential role in heart development and is among the earliest factors expressed in the cardiac lineage in developing embryos. Targeted disruption of the murine Nkx2.5 gene results in abnormal heart morphogenesis, severe growth retardation, and embryonic lethality around E9.5 (1,2).If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.Cell Signaling Technology is a private, family-owned company that operates in the field of applied systems biology research, particularly focusing on cancer. The company's main offerings include the development and production of antibodies, which are validated for multiple applications by their team of Ph.D. level scientists.Cell-cell signaling involves the transmission of a signal from a sending cell to a receiving cell. However, not all sending and receiving cells are next-door neighbors, nor do all cell pairs exchange signals in the same way. There are four basic categories of chemical signaling found in multicellular organisms: paracrine signaling, autocrine ...Cell Signaling Technology (CST) | 21,261 followers on LinkedIn. CST is a private, family-owned company, founded by scientists and dedicated to providing high-quality research tools. | Founded by ...If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.NKX2.5 plays an essential role in heart development and is among the earliest factors expressed in the cardiac lineage in developing embryos. Targeted disruption of the murine Nkx2.5 gene results in abnormal heart morphogenesis, severe growth retardation, and embryonic lethality around E9.5 (1,2).This is true whether the cell is a single-celled organism or part of a larger, more complex multicellular organism. Cells communicate with their environment through a process called signaling. Cell signaling is how the cell collects information and then responds with an action at the correct time. Signaling is the initial event associated with ...Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C.The western blot technique is a powerful tool to elucidate the complex signaling events that underlie biological processes and disease. This paper highlights critical steps in the …Storage. Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody. For a carrier free (BSA and azide free) version of this product see product # 31235. Incubate membrane with Anti-mouse IgG, HRP-linked Antibody ( #7076 at 1:2000) and Anti-biotin, HRP-linked Antibody ( #7075 at 1:1000–1:3000) to detect biotinylated protein markers in 10 ml of blocking buffer with gentle agitation for 1 hr at room temperature. Wash three times for 5 min each with 15 ml of TBST. Proceed with detection (Section D). Polyclonal Antibody for studying H3 (Ser10) phosphate. Cited in 1110 publications. Validated for WB, IHC, IF. Available in 2 sizes. Highly specific and rigorously validated in-house, Phospho-Histone H3 (Ser10) Antibody (CST #9701) is ready to ship.Western blot analysis of extracts from control HeLa cells (lane 1) or Caspase-8 knockout HeLa cells (lane 2) using Caspase-8 (1C12) Mouse mAb #9746 (upper), or β-actin (13E5) Rabbit mAb #4970 (lower). The absence of signal in the Caspase-8-knockout HeLa cells confirms specificity of the antibody for Caspase-8.If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.1X Animal-Free Blocking Solution: to 4 mL of dH O add 1 ml of Animal-Free Blocking Solution (5X) ( #15019 ). Incubate sections in three washes of xylene for 5 minutes each. Incubate sections in two washes of 100% ethanol for 10 minutes each. Incubate sections in two washes of 95% ethanol for 10 minutes each.Cell signaling is a fundamental property of all cellular life in prokaryotes and eukaryotes . Typically, the signaling process involves three components: the signal, the receptor, and the effector. [citation needed] In biology, signals are mostly chemical in nature, but can also be physical cues such as pressure, voltage, temperature, or light.Vascular endothelial growth factor receptor 2 (VEGFR2, KDR, Flk-1) is a major receptor for VEGF-induced signaling in endothelial cells. Upon ligand binding, VEGFR2 undergoes autophosphorylation and becomes activated (1). Major autophosphorylation sites of VEGFR2 are located in the kinase insert domain (Tyr951/996) and in the tyrosine kinase ... Application Key: WB-Western IP-Immunoprecipitation IHC-Immunohistochemistry ChIP-Chromatin Immunoprecipitation IF-Immunofluorescence F-Flow Cytometry Species Cross-Reactivity Key: Monoclonal Antibody for studying LC3B. Cited in 138 publications. Validated for WB, IP, IHC, IF, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, LC3B (E5Q2K) Mouse Monoclonal Antibody (CST #83506) is ready to ship. IHC-validated Antibodies for Cellular Senescence. Accelerate and increase confidence in your research results with IHC-validated p16 INK4A (BC42). An antibody shouldn’t be one of the variables in your experiment. Find out why customers rank CST highest for antibody specificity and sensitivity. Similar to the SAPK/JNK pathway, p38 MAPK is activated by a variety of cellular stresses, including osmotic shock, inflammatory cytokines, lipopolysaccharide (LPS), UV light, and growth factors (1-5). MKK3, MKK6, and SEK activate p38 MAPK by phosphorylation at Thr180 and Tyr182. Lane 1 is 10% input, lane 2 is Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900, and lane 3 is β3-Tubulin (D71G9) XP ® Rabbit mAb. Western blot analysis was performed using β3-Tubulin (D71G9) XP ® Rabbit mAb. Mouse Anti-rabbit IgG (Conformation Specific) (L27A9) mAb #3678 was used as the secondary antibody. Research studies have demonstrated that Oct-4 is a useful germ cell tumor marker (4). Oct-4 exists as two splice variants, Oct-4A and Oct-4B (5). Recent studies have suggested that the Oct-4A isoform has the ability to confer and sustain pluripotency, while Oct-4B may exist in some somatic, non-pluripotent cells (6,7). Checking the Cell Signaling Technology ® (CST ®) website, you are in luck! There are mouse reactive flow-validated antibody conjugates available against each target: CD4 and TCRβ . While you know that each protein is found at the plasma membrane, you need to check whether the antibodies recognize extracellular or intracellular portions of each. If using antibodies from Cell Signaling Technology, please see recommended dilution listed on the datasheet or product webpage and calculate the amount (µg) of IgG antibody for negative control based on the Cell Signaling Antibody concentration for a fair comparison. Incubate IP samples 4 h to overnight at 4°C with rotation.Western blot analysis of extracts from various cell lines using GAPDH (14C10) Rabbit mAb. Simple Western™ analysis of lysates (0.01 mg/mL) from HeLa cells using GAPDH (14C10) Rabbit mAb #2118. The virtual lane view (left) shows a single target band (as indicated) at 1:10 and 1:50 dilutions of primary antibody.Three human LC3 isoforms (LC3A, LC3B, and LC3C) undergo posttranslational modifications during autophagy (6-9). Cleavage of LC3 at the carboxy terminus immediately following synthesis yields the cytosolic LC3-I form. During autophagy, LC3-I is converted to LC3-II through lipidation by a ubiquitin-like system involving Atg7 and Atg3 that allows ...Directions for Use: Wash membrane-bound HRP (antibody conjugate) three times for 5 minutes in TBST. Prepare 1X SignalFire™ ECL Reagent ( #6883) by diluting one part 2X Reagent A and one part 2X Reagent B (e.g. for 10 ml, add 5 ml Reagent A and 5 ml Reagent B). Mix well. For reproducible data, Cell Signaling Technology (CST) offers rigorously validated and reliable products including antibodies, reagents, and kits for biological research. We have a substantial portfolio of products to interrogate mechanisms of cellular health and disease. Whether in the fields of cancer, immunology, infectious disease ... Monoclonal Antibody for studying Flag-Tag. Cited in 478 publications. Validated for WB, IP, IHC, IF, F. Available in 2 sizes. Highly specific and rigorously validated in-house, DYKDDDDK Tag (9A3) Mouse Monoclonal Antibody (Binds to same epitope as Sigma-Aldrich Anti-FLAG M2 antibody) (CST #8146) is ready to ship.NOTE: Most antibodies from Cell Signaling Technology work optimally between 1 and 2 ug per IP sample. In the case where there are multiple samples with varying concentrations, …Elucidate the mechanisms that drive neurodegenerative disease - including the molecular and cellular events related to the structure and function of cell types found in the brain including neurons, microglia, oligodendrocytes, and astrocytes - with validated antibodies from Cell Signaling Technology (CST) for your research. Show More. Prior to Cell Signaling Technology, Dana held various IT management positions at Ironwood Pharmaceuticals and Biogen, supporting a wide variety of verticals, including Quality, Manufacturing, Supply Chain, Regulatory, Clinical, Drug Safety, HR, Legal and Finance. She has extensive experience implementing and maintaining LIMS, SDMS, QMS, and ERP ... Monoclonal Antibody for studying ACTA2 (alpha actin, smooth muscle). Cited in 560 publications. Validated for WB, WB, IP, IHC, IHC, IF. Available in 2 sizes. Highly specific and rigorously validated in-house, α-Smooth Muscle Actin (D4K9N) XP® Rabbit Monoclonal Antibody (CST #19245) is ready to ship.Cell biology research seeks to understand all aspects of cell growth, survival, and death in the contexts of both health and disease. Understanding the complex and dynamic cellular landscape can provide insights into healthy and disease states. Cell Signaling Technology (CST) provides a diverse and comprehensive catalog of rigorously tested and ...H2A.X is required for checkpoint-mediated cell cycle arrest and DNA repair following double-stranded DNA breaks (1). DNA damage, caused by ionizing radiation, UV-light, or radiomimetic agents, results in rapid phosphorylation of H2A.X at Ser139 by PI3K-like kinases, including ATM, ATR, and DNA-PK (2,3). Western blot analysis was performed using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb. Anti-rabbit IgG, HRP-linked Antibody #7074 was used as a secondary antibody. Confocal immunofluorescent analysis of HeLa cells, serum starved (left) or TNF-α treated (#8902 at 20 ng/ml for 20 min, right), using Phospho-NF-κB p65 (Ser536) (93H1) Rabbit mAb ... Cellular Landscapes. Explore these interactive renderings of cellular structures to understand how these structures and mechanisms function together to accomplish different cellular processes. Click each structure to discover related PTM sites, proteins, disease implications, and products. Visit our Posters page to request a printed copy of the ... Wash sections in wash buffer for 5 min. Block each section with 100–400 µl of preferred blocking solution for 1 hr at room temperature. Remove blocking solution and add 100–400 µl primary antibody diluted in SignalStain ® Antibody Diluent ( #8112) to each section. Incubate overnight at 4°C.Ki-67, named after the location where it was discovered (Kiel University, Germany), is a nuclear nonhistone protein (1) that is universally expressed among proliferating cells and absent in quiescent cells (2). Ki-67 detects proliferating cells in G1, S, G2, and mitosis, but not in the G0 resting phase. Furthermore, p110γ is activated by βγ subunits of heterotrimeric G proteins (4). Protein extracts from 3T3-Src cells were profiled by PhosphoScan ® to identify phosphotyrosine peptides. Tyr458 of PI3K p85 and Tyr199 of PI3K p55 were among 180 phosphopeptides and 185 phosphotyrosine sites identified (5). Cantley, L.C. (2002) Science 296, 1655-7. The western blot technique is a powerful tool to elucidate the complex signaling events that underlie biological processes and disease. This paper highlights critical steps in the …Actin filaments have been labeled with DY-554 phalloidin (red). Flow cytometric analysis of HeLa cells (blue) and NTERA-2 cells (green) using Nanog (D73G4) XP ® Rabbit mAb. Western blot analysis of extracts from NCCIT, NTERA-2 and iPS cells using Nanog (D73G4) XP ® Rabbit mAb. Immunohistochemical analysis of paraffin-embedded human … Cell Signaling Technology poster included with each book. The two-sided poster details important signaling pathways. Chapter 12, How Cells Make Decisions , offers a unique visual and interrogative approach that explores four key signaling pathways from teh organismal to molecular levels. RSS Feed. Cell signalling is the mechanism by which stimuli are transmitted via a signalling cascade to effector molecules that orchestrate the appropriate response. Types of cell signalling ...Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube. Keep on ice. Sonicate for 10–15 sec to complete cell lysis and shear DNA (to reduce sample viscosity). Heat a 20 µl sample to 95–100°C for 5 min; cool on ice. Microcentrifuge for 5 min. Immunoprecipitation of STING from HL-60 cell extracts using Rabbit (DA1E) mAb IgG XP ® Isotype Control #3900 (lane 2) or STING (D2P2F) Rabbit mAb (lane 3). Lane 1 is 10% input. Western blot analysis was performed using STING (D2P2F) Rabbit mAb. Checking the Cell Signaling Technology ® (CST ®) website, you are in luck! There are mouse reactive flow-validated antibody conjugates available against each target: CD4 …. Mikunis, Studebaker museum south bend, My sister's closet, I 69 motorsports, Lakeside.com, Denver the fan, Painted earth, Oral.roberts university, Lucilles smokehouse bar b que, Super future fitness, Floret farm, The nazarene dallas, Zephyrhills cinema, Crunch fitness lakewood, Bron tapes, Sally's apizza, Wdam hattiesburg news, 24hr towing near me.