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MAB3402

Sigma-Aldrich

Anti-Glial Fibrillary Acidic Protein Antibody, clone GA5

clone GA5, Chemicon®, from mouse

Synonym(s):

GFAP

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

100

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

GA5, monoclonal

species reactivity

chicken, pig, rat, bovine, mouse, rabbit, human

manufacturer/tradename

Chemicon®

technique(s)

immunocytochemistry: suitable
immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
western blot: suitable

isotype

IgG1

NCBI accession no.

XP_005668766.1

UniProt accession no.

F1RR02

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... GFAP(2670)

General description

Glial fibrillary acidic protein is a class-III intermediate filament. GFAP is the main constituent of intermediate filaments in astrocytes and serves as a cell specific marker that distinguishes differentiated astrocytes from other glial cells during the development of the central nervous system.

Specificity

Expected to cross-react with porcine, chicken, bovine, and rabbit.
The antibody reacts with GFAP from human, pig, chicken and rat. In tissue sections this antibody stains astrocytes and Bergman glia cells (Debus, E., 1983).

Immunogen

Purified Glial Fibrillary Acidic Protein (GFAP) from pig spinal cord (Debus, E., 1983).

Application

Anti-Glial Fibrillary Acidic Protein Antibody, clone GA5 is an antibody against Glial Fibrillary Acidic Protein for use in IC, IH, IH(P) & WB with more than 55 product citations.
Immunocytochemistry:
5 μg/mL of a previous lot was used.

Immunohistochemistry:
5 µg/mL

Immunoblotting:
Recognizes a 51kDa protein in reducing westerns of total brain lysates.

Optimal working dilutions must be determined by end user.
Research Category
Neuroscience
Research Sub Category
Neuronal & Glial Markers

Quality

Routinely evaluated by Western Blot on Mouse brain lysate.

Western Blot Analysis:
1:1000 dilution of this lot detected Glial Fibrillary Acidic Protein on 10 μg of Mouse Brain lysate.

Target description

50 kDa

Linkage

Replaces: 04-1031; 04-1062

Physical form

Format: Purified
Protein A purified
Purified mouse monoclonal IgG1 in buffer containing 0.02 M phosphate buffer, 0.25 M NaCl with 0.1% sodium azide, pH 7.6.

Storage and Stability

Store the reconstituted antibody at 2-8°C for up to 6 months after date of receipt.
DO NOT FREEZE.

Analysis Note

Control
Mouse brain tissue, Astrocyte culture.

Other Notes

2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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The transcriptional coactivator Querkopf controls adult neurogenesis.
Merson, TD; Dixon, MP; Collin, C; Rietze, RL; Bartlett, PF; Thomas, T; Voss, AK
The Journal of Neuroscience null
Selective removal of photoreceptor cells in vivo using the biodegradable elastomer poly(glycerol sebacate).
Ghosh, F; Neeley, WL; Arner, K; Langer, R
Tissue Engineering: Part A null
Innate synchronous oscillations in freely-organized small neuronal circuits.
Shein Idelson, M; Ben-Jacob, E; Hanein, Y
Testing null
Hui Li et al.
Journal of cellular and molecular medicine, 16(7), 1606-1617 (2011-10-19)
Neural tube defects (NTDs) are complex congenital malformations resulting from incomplete neurulation in embryo. Despite surgical repair of the defect, most of the patients who survive with NTDs have a multiple system handicap due to neuron deficiency of the defective
Vladimir V Kalinichenko et al.
Hepatology (Baltimore, Md.), 37(1), 107-117 (2002-12-25)
Previous studies have shown that haploinsufficiency of the splanchnic and septum transversum mesoderm Forkhead Box (Fox) f1 transcriptional factor caused defects in lung and gallbladder development and that Foxf1 heterozygous (+/-) mice exhibited defective lung repair in response to injury.
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