Anti-PCDH19 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-PCDH19 Antibody (CSB-PA844701ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Protocadherin-19 Antibody,PCDH19 Antibody,KIAA1313 Antibody

More alternative names for the antibody
KIAA1313 antibody|PCD19_HUMAN antibody|PCDH19 antibody|Protocadherin 19 antibody|Protocadherin-19 antibody
Anti-PCDH19 antibody – C-terminal (ab191198)
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Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-PCDH19 Antibody

Catalogue No.

CSB-PA844701ESR2HU

Reactivity

Human

Immunogen

Recombinant human Protocadherin-19 protein (568-678AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

126 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:101125719( Gorilla), Entrez Gene:100059478( Horse), Entrez Gene:57526( Human), Entrez Gene:279653( Mouse), Omim:300460( Human), SwissProt:Q8TAB3( Human), SwissProt:Q80TF3( Mouse), Unigene:4993( Human), Unigene:39738( Mouse)

Protein function

Potential calcium-dependent cell-adhesion protein.

Protein tissue specificity

Moderately expressed in all regions of the brain examined, with lowest levels found in the cerebellum. Moderate expression is also found in ovary, and low expression in all other tissues tested. Also detected in primary skin fibroblast. .

Involvement in disease

Epileptic encephalopathy, early infantile, 9 (EIEE9) [MIM:300088]: A condition characterized by seizure with onset in infancy or early childhood, cognitive impairment, and delayed development of variable severity in some patients. Additional features include autistic signs and psychosis. The disorder is sex-limited, with the phenotype being restricted to females. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein cellular localization

Cell membrane ; Single-pass type I membrane protein .

Note

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Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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