GFAP Rabbit pAb

-YT1894

Catalog: YT1894
Size
Price
Status
Qty.
200μL
$450.00
4 weeks

0

100μL
$280.00
4 weeks

0

40μL
$150.00
4 weeks

0

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Main Information
Target

GFAP

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, IHC, IF, ELISA

MW

50kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-1:2000; IHC 1:100-1:300; IF 1:200-1:1000; ELISA 1:5000; Not yet tested in other applications.
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
GFAP Polyclonal Antibody detects endogenous levels of GFAP protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year (Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
50kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human GFAP. AA range:11-60
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Specificity:
GFAP Polyclonal Antibody detects endogenous levels of GFAP protein.
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Gene Name:
GFAP
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Protein Name:
Glial fibrillary acidic protein
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Other Name:
GFAP ;
Glial fibrillary acidic protein ;
GFAP
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Database Link:
Organism Gene ID SwissProt
Human 2670; P14136;
Mouse 14580; P03995;
Rat 24387; P47819;
Background:
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. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq , Oct 2008] ,
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Function:
Alternative products:Isoforms differ in the C-terminal region which is encoded by alternative exons ,Disease:Defects in GFAP are a cause of Alexander disease (ALEXD) [MIM:203450]. Alexander disease is a rare disorder of the central nervous system. It is a progressive leukoencephalopathy whose hallmark is the widespread accumulation of Rosenthal fibers which are cytoplasmic inclusions in astrocytes. The most common form affects infants and young children , and is characterized by progressive failure of central myelination , usually leading to death usually within the first decade. Infants with Alexander disease develop a leukoencephalopathy with macrocephaly , seizures , and psychomotor retardation. Patients with juvenile or adult forms typically experience ataxia , bulbar signs and spasticity , and a more slowly progressive course. ,Function:GFAP , a class-III intermediate filament , is a cell-specific marker that , during the development of the central nervous system , distinguishes astrocytes from other glial cells. ,online information:GFAP entry ,similarity:Belongs to the intermediate filament family. ,subcellular location:Associated with intermediate filaments. ,subunit:Interacts with SYNM (By similarity) . Isoform 3 interacts with PSEN1 (via N-terminus) . ,tissue specificity:Expressed in cells lacking fibronectin. ,
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Cellular Localization:
Cytoplasm . Associated with intermediate filaments. .
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Tissue Expression:
Research Areas:
>>JAK-STAT signaling pathway
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Catalog: YT1894
Size
Price
Status
Qty.
200μL
$450.00
4 weeks

0

100μL
$280.00
4 weeks

0

40μL
$150.00
4 weeks

0

Add to cart

Collected

Collect

Customized Service

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