|Positive WB detected in||rat brain tissue, human brain tissue, pig brain tissue, U-251 cells, rat cerebellum, mouse brain, mouse cerebellum, rabbit brain|
|Positive IP detected in||mouse brain tissue|
|Positive IHC detected in||human brain tissue, human gliomas tissue, mouse brain tissue, rat brain tissue|
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
|Western Blot (WB)||WB : 1:5000-1:50000|
|Immunoprecipitation (IP)||IP : 0.5-4.0 ug for IP and 1:500-1:2000 for WB|
|Immunohistochemistry (IHC)||IHC : 1:500-1:10000|
|Sample-dependent, check data in validation data gallery|
This antibody is not recommended for immunocytofluorescent assays. It is not suitable for frozen sections.
60190-1-Ig targets GFAP in WB, IP, IHC,ELISA applications and shows reactivity with human, mouse, rat, pig, rabbit samples.
|Tested Reactivity||human, mouse, rat, pig, rabbit|
|Cited Reactivity||human, mouse, rabbit, rat|
|Host / Isotype||Mouse / IgG2a|
|Immunogen||GFAP fusion protein Ag10452|
|Full Name||glial fibrillary acidic protein|
|Calculated molecular weight||432 aa, 50 kDa|
|Observed molecular weight||45-52 kDa|
|GenBank accession number||BC013596|
|Gene ID (NCBI)||2670|
|Purification Method||Protein A purification|
|Storage Buffer||PBS with 0.02% sodium azide and 50% glycerol pH 7.3.|
|Storage Conditions||Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.|
FunctionGFAP (Glial fibrillary acidic protein) is a type III intermediate filament (IF) protein specific to the central nervous system (CNS). GFAP is one of the main components of the intermediate filament network in astrocytes and has been proposed as playing a role in cell migration, cell motility, maintaining mechanical strength, and in mitosis.
Tissue specificityGFAP is expressed in central nervous system cells, predominantly in astrocytes. GFAP is commonly used as an astrocyte marker. However, GFAP is also present in peripheral glia and in non-CNS cells, including fibroblasts, chondrocytes, lymphocytes, and liver stellate cells (PMID: 21219963).
Involvement in disease
- Mutations in GFAP lead to Alexander disease (OMIM: 203450), an autosomal dominant CNS disorder. The mutations present in affected individuals are thought to be gain-of-function.
- Upregulation of GFAP is a hallmark of reactive astrocytes, in which GFAP is present in hypertrophic cellular processes. Reactive astrogliosis is present in many neurological disorders, such as stroke, various neurodegenerative diseases (including Alzheimer's and Parkinson's disease), and neurotrauma.
IsoformsAstrocytes express 10 different isoforms of GFAP that differ in the rod and tail domains (PMID: 25726916), which means that they differ in molecular size. Isoform expression varies during the development and across different subtypes of astrocytes. Not all isoforms are upregulated in reactive astrocytes.
Post-translational modificationsIntermediate filament proteins are regulated by phosphorylation. Six phosphorylation sites have been identified in GFAP protein, at least some of which are reported to control filament assembly (PMID: 21219963).
Cellular localizationGFAP localizes to intermediate filaments and stains well in astrocyte cellular processes.
|Product Specific Protocols|
|WB protocol for GFAP antibody 60190-1-Ig||Download protocol|
|IHC protocol for GFAP antibody 60190-1-Ig||Download protocol|
|IF protocol for GFAP antibody 60190-1-Ig||Download protocol|
|IP protocol for GFAP antibody 60190-1-Ig||Download protocol|
|Click here to view our Standard Protocols|
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The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.
Mai (Verified Customer) (01-30-2020)
The antibody seemed to have some background. I will repeat the experiment with different dilutions and conditions to find an optimum dilution for this antibody.
George (Verified Customer) (08-27-2019)
This gave good staining for activated astrocytes in the 488 channel (1:500 secondary dilution) however there was also significant endogenous background staining which made analysis difficult.
Chintan (Verified Customer) (06-03-2019)
This antibody was used to detect Glial fibrillary acidic protein in primary mouse microglia cells using Western blot. Antibody worked quite well and gave a very specific band near 50 kDa.
Di (Verified Customer) (12-18-2018)
Lalitha (Verified Customer) (12-13-2018)
Chandrakanth (Verified Customer) (12-06-2018)
Emily (Verified Customer) (11-29-2018)