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Mouse Anti-ATOH7 Recombinant Antibody (1A5) (CBMAB-A0598-LY)

The product is antibody recognizes ATOH7. The antibody 1A5 immunoassay techniques such as: WB, ELISA.
See all ATOH7 antibodies
Published Data

Summary

Host Animal
Mouse
Specificity
Human
Clone
1A5
Antibody Isotype
IgG2a, κ
Application
WB, ELISA

Basic Information

Immunogen
ATOH7 (NP_660161, 53 a.a. ~ 99 a.a) partial recombinant protein with GST tag.
Specificity
Human
Antibody Isotype
IgG2a, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS, pH 7.4
Preservative
None
Concentration
Batch dependent
Purity
> 95% Purity determined by SDS-PAGE.
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.

Target

Full Name
atonal homolog 7 (Drosophila)
Introduction
ATOH7 is a member of the family of basic helix-loop-helix (bHLH) proteins with similarity to Drosophila 'atonal,' a proneural bHLH gene that controls photoreceptor development (Brown et al., 2002 [PubMed 11889557]).[supplied by OMIM
Entrez Gene ID
UniProt ID
Alternative Names
Math5; bHLHa13
Function
Transcription factor that positively regulates the determination of retinal ganglion cell fate and formation of the optic nerve and retino-hypothalamic tract (By similarity).
Required for retinal circadian rhythm photoentrainment (By similarity).
Biological Process
Circadian rhythm Source: Ensembl
Entrainment of circadian clock by photoperiod Source: UniProtKB
Neural retina development Source: MGI
Neuron differentiation Source: GO_Central
Optic nerve development Source: MGI
Regulation of transcription by RNA polymerase II Source: GO_Central
Cellular Location
Nucleus
Involvement in disease
Persistent hyperplastic primary vitreous, autosomal recessive (PHPVAR): The disease is caused by variants 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). 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.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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