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GFAP Rabbit Polyclonal Antibody (APC)

CAT: 0013-GTR18525492Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18525492Size:100 µg
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Description
GFAP Rabbit Polyclonal Antibody (APC)
Product Name Alternative
Glial fibrillary acidic protein; GFAP; GFAP
UniProt
P14136
Reactivity
Human, Mouse, Rat
Cross Reactivity
No cross-reactivity with other proteins
Immunogen
E.coli-derived human GFAP recombinant protein (Position: Q93-M432) . Human GFAP shares 94% amino acid (aa) sequence identity with both mouse and rat GFAP.
Target
Glial fibrillary acidic protein
Clonality
Polyclonal
Conjugation
APC
Field of Research
Cell Biology, Disease Biomarkers, Neuroscience, Signal Transduction, Stem Cell & Developmental Biology
Purification
Immunogen affinity purified.
Dilution
Optimal dilutions should be determined by end users.
Form
Liquid
Molecular Weight
49880 Da
Storage Conditions
At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
Notes
For research use only.
Applications Notes
Recommended applications are based on the parent unconjugated antibody. Customers may select suitable applications according to their experimental needs.
Host or Source
Rabbit
Preservative
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Isotype
Rabbit IgG

UniProtKB · P14136

Glial fibrillary acidic protein

GFAP_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P14136
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GFAP
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
GFAP
EC number
—
Processing
—
Secondary accessions
A7REI1, B2RD44, D3DX59, E9PAX3, Q53H98, Q5D055, Q6ZQS3, Q7Z5J6, Q7Z5J7, Q96KS4, Q96P18, Q9UFD0
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

PTM

CitrullinationMethylationPhosphoprotein

Domain

Coiled coil

Cellular component

CytoplasmIntermediate filament

Disease

Disease variantLeukodystrophy

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