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ASCL1 antibody (AA 63-90)
This anti-ASCL1 antibody is a Rabbit Polyclonal antibody detecting ASCL1 in WB and ELISA. Suitable for Human.
Quick Overview for ASCL1 antibody (AA 63-90) (ABIN3029829)
Target
See all ASCL1 Antibodies
ASCL1
(Achaete-Scute Complex Homolog 1 (Drosophila) (ASCL1))
Reactivity
All reactivities for ASCL1 antibodies
Human
Host
All hosts for ASCL1 antibodies
Rabbit
Clonality
All clonalities for ASCL1 antibodies
Polyclonal
Conjugate
All conjugates for ASCL1 antibodies
This ASCL1 antibody is un-conjugated
Application
All applications for ASCL1 antibodies
Western Blotting (WB), ELISA
Product Details anti-ASCL1 Antibody
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Binding Specificity
All epitopes for ASCL1 antibodies
AA 63-90
Purification
Antigen affinity purified
Immunogen
A portion of amino acids 63-90 from the human protein was used as the immunogen for this MASH1 / ASCL1 antibody.
Isotype
Ig Fraction
Alternatives
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Application Details
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Application Notes
Titration of the ASCL1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
In 1X PBS, pH 7.4, with 0.09 % sodium azide
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Aliquot the ASCL1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
Target Details for ASCL1
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Target
ASCL1
(Achaete-Scute Complex Homolog 1 (Drosophila) (ASCL1))
Alternative Name
ASCL1 (MASH1)
Background
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.
UniProt
P50553
Pathways
Dopaminergic Neurogenesis
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