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GFAP antibody (N-Term)
GFAP
Reactivity: Human
WB
Host: Rabbit
Polyclonal
RB2895
unconjugated
Product Details anti-GFAP Antibody
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Target
See all GFAP Antibodies
GFAP
(Glial Fibrillary Acidic Protein (GFAP))
Binding Specificity
All epitopes for GFAP antibodies
AA 10-40, N-Term
Reactivity
All reactivities for GFAP antibodies
Human
Host
All hosts for GFAP antibodies
Rabbit
Clonality
All clonalities for GFAP antibodies
Polyclonal
Conjugate
All conjugates for GFAP antibodies
This GFAP antibody is un-conjugated
Application
All applications for GFAP antibodies
Western Blotting (WB)
Purification
This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
Immunogen
This GFAP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 10-40 amino acids from the N-terminal region of human GFAP.
Clone
RB2895
Isotype
Ig Fraction
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Discover our top product GFAP Primary Antibody
Alternatives
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Application Details
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Application Notes
WB: 1:1000. WB: 1:8000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
Expiry Date
6 months
Target Details for GFAP
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Target
GFAP
(Glial Fibrillary Acidic Protein (GFAP))
Alternative Name
GFAP (GFAP Products )
Synonyms
GFAP antibody, AI836096 antibody, cb345 antibody, etID36982.3 antibody, gfapl antibody, wu:fb34h11 antibody, wu:fk42c12 antibody, xx:af506734 antibody, zgc:110485 antibody, glial fibrillary acidic protein antibody, GFAP antibody, LOC100136168 antibody, gfap antibody, Gfap antibody
Background
GFAP is 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.
Molecular Weight
49880
Gene ID
2670
NCBI Accession
NP_001124491 , NP_001229305 , NP_002046
UniProt
P14136
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