Anti-ATOH7 Antibody

$99.00$319.00

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

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Rabbit Anti-ATOH7 Antibody (CSB-PA850773ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Protein atonal homolog 7 Antibody,Class A basic helix-loop-helix protein 13 Antibody,bHLHa13 Antibody,Helix-loop-helix protein hATH-5 Antibody,hATH5 Antibody,ATOH7 Antibody,ATH5 Antibody,BHLHA13 Antibody

More alternative names for the antibody
ATOH7 antibody|ATOH7_HUMAN antibody|Atonal homolog 7 (Drosophila) antibody|Atonal Homolog 7 antibody|bHLHa13 antibody|Class A basic helix-loop-helix protein 13 antibody|hATH5 antibody|Helix-loop-helix protein hATH-5 antibody|Math5 antibody|Protein atonal homolog 7 antibody
Anti-MATH5 antibody (ab13536)
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Recommended applications: ELISA, IHC

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

Recommended protocols: check protocols

Name

Anti-ATOH7 Antibody

Catalogue No.

CSB-PA850773ESR1HU

Reactivity

Human

Immunogen

Recombinant human Protein atonal homolog 7 protein (47-152AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

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

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

16 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:220202( Human), Entrez Gene:53404( Mouse), Entrez Gene:365564( Rat), Omim:609875( Human), SwissProt:Q8N100( Human), SwissProt:Q9Z2E5( Mouse), Unigene:175396( Human), Unigene:228661( Mouse)

Protein function

Transcription factor involved in the differentiation of retinal ganglion cells. .

Involvement in disease

Persistent hyperplastic primary vitreous, autosomal recessive (PHPVAR) [MIM:221900]: A developmental eye malformation associated with microphthalmia, cataract, glaucoma, and congenital retinal non-attachment. It is due to failure of the primary vitreous to regress in utero, resulting in the presence of a retrolental fibrovascular membrane with persistence of the posterior portion of the tunica vasculosa lentis and hyaloid artery. Disease manifestations range from a trivial remnant of hyaloid vessels to a dense fibrovascular mass causing lens opacity and retinal detachment. . Note=The disease is caused by mutations affecting the gene represented in this entry. A 6.5 kb deletion that spans a remote cis regulatory element 20 kb upstream from ATOH7 has been found in PHPVAR patients (PubMed:21441919). .

Protein cellular localization

Nucleus .

Note

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Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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