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Human/Rat GFAP Affinity Purified Polyclonal Ab (25 UG)

货号: AF2594-SP 基本售价: 1378.1 元 规格: -

产品信息

概述
货号AF2594-SP
别名FLJ45472; GFAP astrocytes; glial fibrillary acidic protein
全称Glial Fibrillary Acidic Protein
反应种属Human/Rat
应用Western Blot(0.2 µg/mL)
Simple Western(0.1-2 µg/mL)
Immunocytochemistry(5-15 µg/mL)
目标/特异性Detects human and rat GFAP in Western blots.
使用方法Western Blot: 0.2 µg/mL
Simple Western: 0.1-2 µg/mL
Immunocytochemistry: 5-15 µg/mL
来源Reconstitute at 0.2 mg/mL in sterile PBS.
产品组分
性能
供应商R&D Systems
Entrez Gene IDs2670 (Human); 14580 (Mouse); 24387 (Rat)
应用文献
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

Dose-dependent changes in neuroinflammatory and arachidonic acid cascade markers with synaptic marker loss in rat lipopolysaccharide infusion model of neuroinflammation.
BMC Neurosci, 2012;13(0):50.
Species: Rat
Sample Type: Tissue Homogenates
Application: WB
TNFalpha-induced AMPA-receptor trafficking in CNS neurons; relevance to excitotoxicity?
Authors: Leonoudakis D, Braithwaite SP, Beattie MS, Beattie EC
Neuron Glia Biol., 2004;1(3):263-273.
Species: Rat
Sample Type: Whole Cells
Application: ICC

纯化方式Antigen Affinity-purified
免疫原E. coli-derived recombinant human GFAP
Leu292-Met432
Accession # P14136
生物活性Human, Rat
标记Unconjugated
溶解方法Reconstitute at 0.2 mg/mL in sterile PBS.
背景

GFAP (Glial fibrillary acidic protein) is a type III intermediate filament protein. It is the major component of astrocyte intermediate filament. Defects in GFAP are a cause of Alexander disease. Alexander disease is a rare disorder of the central nervous system. It is a progressive leukoencephalopathy whose hallmark is the widespread accumulation of Rosenthal fibers which are cytoplasmic inclusions in astrocytes. At the amino acid sequence level, human GFAP shares 91% and 90% identity with rat and mouse GFAP, respectively.

运输条件Blue Ice
存放说明4℃
参考文献
  • Adult Neurogenesis
  • Cancer Biomarkers
  • Glial Lineage Markers
  • ICC / IHC Images: GFAP
  • Intermediate Filaments
  • Neural Progenitor Cell Markers
  • Neural Stem Cell Markers
  • Neural Stem Cells
  • Neuroinflammation
参考图片
Detection of Human and Rat GFAP by Western Blot. Western blot shows lysates of rat cortical stem cells, rat brain tissue, human brain (cortex) tissue, and human brain (hypothalamus) tissue. PVDF membrane was probed with 0.2 µg/mL of Sheep Anti-Human GFAP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2594) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). Specific bands were detected for GFAP at approximately 35-50 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
GFAP in Rat Astrocytes. GFAP was detected in immersion fixed rat astrocytes using 10 µg/mL Sheep Anti-Human GFAP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2594) for 3 hours at room temperature. Cells were stained with the NorthernLights™ 557-conjugated Anti-Sheep IgG Secondary Antibody (red; Catalog # NL010) and counterstained with DAPI (blue). View our protocol for Fluorescent ICC Staining of Cells on Coverslips.
beta ‑III Tubulin in Rat Cortical Neurons and GFAP in Rat Astrocytes. beta ‑III Tubulin was detected in rat cortical neurons using 5 µg/mL Mouse Anti-neuron-specific Mouse beta ‑III Tubulin Monoclonal (clone TuJ‑1) Antibody (Catalog # MAB1195). GFAP was detected in rat astrocytes using 10 µg/mL Sheep Anti-Human GFAP Antigen Affinity-purified Poly­clonal Antibody (Catalog # AF2594). Cells were incubated with primary antibodies for 3 hours at room temperature. Cells were stained for beta‑III Tubulin using the Northern­Lights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # NL007) and for GFAP using the Northern­Lights 493-conjugated Anti-Sheep IgG Secondary Antibody (green; Catalog # NL012). View our protocol for Fluorescent ICC Staining of Cells on Coverslips.
GFAP in Rat Cortical Stem Cells. GFAP was detected in immersion fixed 7 days differentiated rat cortical stem cells using Sheep Anti-Human GFAP Antigen Affinity-purified Poly­clonal Antibody (Catalog # AF2594) at 10 µg/mL for 3 hours at room temperature. Cells were stained using the Northern­Lights™ 557-conjugated Anti-Sheep IgG Secondary Antibody (yellow; Catalog # NL010) and counterstained with DAPI (blue). View our protocol for Fluorescent ICC Staining of Cells on Coverslips.
Detection of Human GFAP by Simple WesternTM. Simple Western lane view shows lysates of human brain (cerebellum) tissue, loaded at 0.2 mg/mL. A specific band was detected for GFAP at approximately 51 kDa (as indicated) using 0.1 µg/mL of Sheep Anti-Human/Rat GFAP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2594) followed by 1:50 dilution of HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.
Detection of Rat GFAP by Simple WesternTM. Simple Western lane view shows lysates of rat brain tissue, loaded at 0.2 mg/mL. A specific band was detected for GFAP at approximately 55 kDa (as indicated) using 2 µg/mL of Sheep Anti-Human/Rat GFAP Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2594) followed by 1:50 dilution of HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). This experiment was conducted under reducing conditions and using the
12-230 kDa separation system.