Product: GFAP Antibody
Catalog: AF6166
Description: Rabbit polyclonal antibody to GFAP
Application: WB
Cited expt.: WB
Reactivity: Human, Mouse, Rat
Prediction: Bovine, Horse
Mol.Wt.: 50kDa; 50kD(Calculated).
Uniprot: P14136
RRID: AB_2835032
Lead Time: Same day delivery
For pricing and ordering contact: Local distributors
MSDS
Data Sheet
COA
WB Handbook
IHC Protocol
IF/ICC Protocol
Source: Rabbit
Application: WB 1:500-1:2000
Reactivity: Human,Mouse,Rat
Prediction: Bovine(100%), Horse(100%)
Clonality: Polyclonal
Specificity: GFAP Antibody detects endogenous levels of total GFAP.
Cite Format: Affinity Biosciences Cat# AF6166, RRID:AB_2835032.
Conjugate: Unconjugated.
Purification: The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
Storage: Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
Alias: wu:fb34h11; ALXDRD; cb345; etID36982.3; FLJ42474; FLJ45472; GFAP; GFAP_HUMAN; gfapl; Glial fibrillary acidic protein; Intermediate filament protein; wu:fk42c12; xx:af506734; zgc:110485;
Immunogen: A synthesized peptide derived from human GFAP, corresponding to a region within N-terminal amino acids.
Uniprot: P14136(GFAP_HUMAN)
Gene(ID): GFAP(2670)
Expression: P14136 GFAP_HUMAN: Expressed in cells lacking fibronectin.
Description: This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. An additional transcript variant has been described, but its full length sequence has not been determined.
Sequence: P14136 GFAP_HUMAN:
