ATOH7 Antibody

Code CSB-PA850773ESR2HU
Size US$166
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  • Immunohistochemistry of paraffin-embedded human colon cancer using CSB-PA850773ESR2HU at dilution of 1:100

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) ATOH7 Polyclonal antibody
Uniprot No.
Target Names
ATOH7
Alternative Names
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
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Protein atonal homolog 7 protein (47-152AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Polyclonal
Isotype
IgG
Purification Method
Antigen Affinity Purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Form
Liquid
Tested Applications
ELISA, IHC
Recommended Dilution
Application Recommended Dilution
IHC 1:20-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Transcription factor that positively regulates the determination of retinal ganglion cell fate and formation of the optic nerve and retino-hypothalamic tract. Required for retinal circadian rhythm photoentrainment.
Gene References into Functions
  1. In conclusion, we have identified a homozygous mutation in the ATOH7 gene in a patient with nonsyndromic congenital retinal nonattachment. PMID: 26933893
  2. We evaluated 21 consanguineous NCRNA pedigrees and identified the causal mutations in known retinal genes in 13 out of our 21 families. We found mutations in ATOH7 in three families. PMID: 28192794
  3. We discovered a novel SNP, rs56238729 (P = 1.22 x 10-13), in the ATOH7-PBLD region that is significantly associated with VCDR in Latino individuals. PMID: 28061514
  4. The genotype and allele frequencies of the polymorphism in ATOH7 did not show any statistically significant association with primary open angle glaucomacompared to controls. PMID: 27617586
  5. Familial linkage studies for primary angle-closure glaucoma have been performed and identified ATOH7 causative primary angle-closure glaucoma disease PMID: 26497787
  6. Single nucleotide polymorphism in ATOH7 gene is associated with primary open angle glaucoma. PMID: 25798827
  7. The significant association of three common variants in TMCO1, ATOH7, and CAV1 with primary open angle, primary angle closure, and pseudoexfoliation glaucoma was found in Pakistani cohorts. PMID: 25489222
  8. Mutations within the ATOH7 gene are not implicated in the pathogenesis of optic nerve hypoplasia in our patient cohort. PMID: 23802135
  9. This study finds that ATOH7 is associated with optic disc size but not independently with cup/disk ratio. PMID: 24457358
  10. a bHLH mutation in ATOH7 causes recessive persistent hyperplasia of the primary vitreous PMID: 22645276
  11. findings document Mendelian mutations within ATOH7 and imply a role for this molecule in the development of structures at the front as well as the back of the eye; study provides further insights into the function of ATOH7, especially its importance in retinal vascular development and hyaloid regression PMID: 22068589
  12. combination of ATOH7 and RFTN1 SNPs increased risk to POAG, indicating their diversified effects in the complex genetics of glaucoma. PMID: 22222511
  13. Report Math5 expression/function in retinal ganglion cells. PMID: 22019371
  14. ATOH7 is significantly associated with open-angle glaucoma. PMID: 21427129
  15. Polymorphisms of ATOH7, TGFBR3 and CARD10 influence the size of optic disc area. PMID: 21307088
  16. This study demonistrated that Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. PMID: 21441919
  17. Genome-wide association identifies ATOH7 as a major gene determining human optic disc size PMID: 20395239

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Involvement in disease
Persistent hyperplastic primary vitreous, autosomal recessive (PHPVAR)
Subcellular Location
Nucleus.
Database Links

HGNC: 13907

OMIM: 221900

KEGG: hsa:220202

STRING: 9606.ENSP00000362777

UniGene: Hs.175396

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