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ATOH1 Recombinant Rabbit mAb (S-1301-11)
ATOH1 Recombinant Rabbit mAb (S-1301-11)
Origin of place Singapore
Model S0B0846-25μl
Supplier ANT BIO PTE.LTD.
Price 100
Hits 1
Updated 8/27/2025
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Product Specification


HostRabbit
AntigenATOH1
SynonymsTranscription factor ATOH1, Atonal bHLH transcription factor 1, Class A basic helix-loop-helix protein 14 (bHLHa14), Helix-loop-helix protein hATH-1 (hATH1), Protein atonal homolog 1, ATH1, BHLHA14
ImmunogenSynthetic Peptide
LocationNucleus
AccessionQ92858
Clone NumberS-1301-11
Antibody TypeRecombinant mAb
IsotypeIgG
ApplicationWB
ReactivityHu, Ms, Rt
Predicted ReactivityCz
PurificationProtein A
Concentration0.5 mg/ml
ConjugationUnconjugated
Physical AppearanceLiquid
Storage BufferPBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
Stability & Storage

12 months from date of receipt / reconstitution, -20 °C as supplied

Dilution


applicationdilutionspecies
WB1:1000

Background

ATOH1 (Atonal homolog 1), also known as MATH1, is a pivotal transcription factor involved in neural development. ATOH1 plays a critical role in neuronal differentiation during neural development. It regulates the differentiation of neural progenitor cells into neurons, facilitating the formation and directed growth of neurons. By modulating the expression of neurodevelopmental genes, ATOH1 influences the fate determination and differentiation processes of neural progenitor cells. The expression of ATOH1 is intimately linked to the development of sensory organs within the inner ear, particularly those related to hearing and balance. Studies have shown that ATOH1 expression is upregulated in response to hair cell damage, making it a key gene in hair cell regeneration. Overexpression of ATOH1 can induce hair cell regeneration in the cochlear sensory epithelium and non-sensory epithelia. ATOH1 is also involved in cell regeneration in multiple systems. For instance, in the colon, ATOH1-secreting progenitor cells contribute to the regeneration of Lgr5+ stem cells, facilitating the repair of damaged colon tissue through mechanisms independent of the Lgr5+ stem cell lineage.

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