Mouse Monoclonal GFAP antibody [6A6] (STJ98106)

$379.00

Reactivity: Human
Applications: WB, IHC, IF, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Mouse Monoclonal GFAP antibody [6A6] (STJ98106)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, IHC, IF, ELISA

Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; ELISA 1:10000

Recommended protocols: check protocols

Image descriptions:

Click or hover above images to see image description for GFAP Monoclonal Antibody.

Alternative names:

Check alternative names for the antibody

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GFAP antibody,|wu:fb34h11 antibody|ALXDRD antibody|cb345 antibody|etID36982.3 antibody|FLJ42474 antibody|FLJ45472 antibody|GFAP antibody|GFAP_HUMAN antibody|gfapl antibody|Glial fibrillary acidic protein antibody|Intermediate filament protein antibody|wu:fk42c12 antibody|xx:af506734 antibody|zgc:110485 antibody|Anti-GFAP antibody (ab53554)
SCBT cat No: sc-32955|

 

Name

GFAP Monoclonal Antibody

Catalogue No.

STJ98106

Reactivity

Human

Specificity

GFAP Monoclonal Antibody detects endogenous levels of GFAP protein.

Immunogen

Purified recombinant fragment of human GFAP expressed in E Coli

Host

Mouse

Applications

WB, IHC, IF, ELISA

Recommended dilution

WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; ELISA 1:10000

Clonality

Monoclonal

Conjugation

Unconjugated

Isotype

IgG1

Formulation

GFAP Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.

Concentration

1 mg/ml

Purification

GFAP Antibody was purified using affinity purification.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Glial fibrillary acidic protein antibody, GFAP antibody

Database links

Human UniProt/Swiss-Prot:P14136;Mouse UniPort/Swiss-Prot: P03995;Rat UniProt/Swiss-Port: P47819;Human Entrez Gene: 2670;Mouse Entrez Gene: 14580;Rat Entrez Gene: Rn.91512

Protein names

Glial fibrillary acidic protein , GFAP

Protein 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.

Protein tissue specificity

Expressed in cells lacking fibronectin.

Involvement in disease

Alexander disease (ALXDRD) [MIM:203450]: A rare disorder of the central nervous system. The most common form affects infants and young children, and is characterized by progressive failure of central myelination, usually leading to death within the first decade. Infants with Alexander disease develop a leukodystrophy 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. Histologically, Alexander disease is characterized by Rosenthal fibers, homogeneous eosinophilic inclusions in astrocytes. . Note: The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the intermediate filament family.

Protein post-translational modifications

Phosphorylated by PKN1.

Protein cellular localization

Cytoplasm

Research area

All research areas>Structural Proteins>GFAP
(View all antibody categories related to Structural Proteins)

Note

AntibodyPlus can customize GFAP Antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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