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NSJ Bioreagents

SKU:F47525-0.08ML

ASCL1 Antibody / MASH1

ASCL1 Antibody / MASH1

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This gene encodes 'Achaete scute complex homolog like 1' (ASCL1) or 'Mammalian achaete scute complex homolog 1' (MASH1), a member of the basic helix-loop-helix (BHLH) family of transcription factors. The protein activates transcription by binding to the E box (5'-CANNTG-3'). Dimerization with other BHLH proteins is required for efficient DNA binding. This protein plays a role in the neuronal commitment and differentiation and in the generation of olfactory and autonomic neurons. Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases.

Specifications

Family Primary antibody
Formulation In 1X PBS, pH 7.4, with 0.09% sodium azide
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit Ig
Species Reactivity Human
Application WB, ELISA
Application Details Western blot: 1:1000
Application Note Titration of the ASCL1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.
Immunogen A portion of amino acids 63-90 from the human protein was used as the immunogen for this MASH1 / ASCL1 antibody.
Purity Antigen affinity
Storage Aliquot the ASCL1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
Limitation This ASCL1 antibody is available for research use only.
Uniprot # P50553
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/ascl1-antibody-mash1-f47525
Title ASCL1 Antibody / MASH1
Description This gene encodes 'Achaete scute complex homolog like 1' (ASCL1) or 'Mammalian achaete scute complex homolog 1' (MASH1), a member of the basic helix-loop-helix (BHLH) family of transcription factors. The protein activates transcription by binding to the E box (5'-CANNTG-3'). Dimerization with other BHLH proteins is required for efficient DNA binding. This protein plays a role in the neuronal commitment and differentiation and in the generation of olfactory and autonomic neurons. Mutations in this gene may contribute to the congenital central hypoventilation syndrome (CCHS) phenotype in rare cases.
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