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NeuroD1 antibody - 503 003

NeuroD1 is a transcription factor involved in neuronal differentiation and development
Rabbit polyclonal purified antibody
Cat. No.: 503 003
Amount: 50 µg
Price: $375.00
Cat. No. 503 003 50 µg specific antibody, lyophilized. Affinity purified with the immunogen. Albumin and azide were added for stabilization. For reconstitution add 50 µl H2O to get a 1mg/ml solution in PBS. Then aliquot and store at -20°C to -80°C until use.
Antibodies should be stored at +4°C when still lyophilized. Do not freeze!
Applications
 
WB: 1 : 1000 (AP-staining) gallery  
IP: not tested yet
ICC: 1 : 1000 up to 1 : 2000 gallery  
IHC: 1 : 2000 (see remarks) gallery  
IHC-P: 1 : 1000 up to 1 : 4000 gallery  
Immunogen Recombinant protein corresponding to the N-terminal part of mouse NeuroD1 (UniProt Id: Q60867)
Reactivity Reacts with: mouse (Q60867), rat (Q64289).
Other species not tested yet.
Remarks

IHC: Antigen retrieval (citrate buffer pH 6) can be used to improve the signal in immunohistochemical staining.

Data sheet 503_003.pdf
Cat. No.: 503 003
Amount: 50 µg
Price: $375.00
Background

NeuroD1, also referred to as Neurogenic differentiation factor 1 or BETA2, is a member of the basic helix-loop-helix (bHLH) family of transcription factors. It forms heterodimers with other bHLH proteins and activates transcription of genes with E box-containing promoters. It is expressed in the developing brain and pancreas as well as in differentiating neurons in both the central and peripheral nervous system (1, 2, 3).
NeuroD1 acts as a differentiation factor during neurogenesis (1, 4). It regulates the development of the mammalian retina, inner ear sensory neurons, granule cells forming either the cerebellum or the dentate gyrus cell layer of the hippocampus (1, 2, 3), endocrine islet cells of the pancreas and enteroendocrine cells of the small intestine (5).
Mice lacking NeuroD1 become severely diabetic, show several developmental and functional defects throughout the body, and die shortly after birth (1,2,5).
Human mutations have been linked to a number of types of diabetes, including type I diabetes mellitus and maturity-onset diabetes of the young (1).