Neuro D (phospho Ser274) rabbit pAb

Neuro D (phospho Ser274) rabbit pAb

AO-06-ES6360-50

Neuro D (phospho Ser274) rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES6360
Product nameNeuro D (phospho Ser274) rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC
Other nameNEUROD1; BHLHA3; NEUROD; Neurogenic differentiation factor 1; NeuroD; NeuroD1; Class A basic helix-loop-helix protein 3; bHLHa3
Size50μL
Unit price ($)148
Human gene ID4760
Human Swiss-ProtQ13562
SourceRabbit
IsotypeIgG
TargetNeuro D
Fields>>Maturity onset diabetes of the young
Gene nameNEUROD1
Protein nameNeurogenic differentiation factor 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID18012
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ60867
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID29458
Rat gene linkView Rat Gene
Rat Swiss-ProtQ64289
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human Neuro D around the phosphorylation site of Ser274. AA range:240-289
SpecificityPhospho-Neuro D (S274) Polyclonal Antibody detects endogenous levels of Neuro D protein only when phosphorylated at S274.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000;IHC-p 1:50-300
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)36kD
BackgroundThis gene encodes a member of the NeuroD family of basic helix-loop-helix (bHLH) transcription factors. The protein forms heterodimers with other bHLH proteins and activates transcription of genes that contain a specific DNA sequence known as the E-box. It regulates expression of the insulin gene, and mutations in this gene result in type II diabetes mellitus. [provided by RefSeq, Jul 2008],
Functiondisease:Defects in NEUROD1 are the cause of maturity onset diabetes of the young type 6 (MODY6) [MIM:606394]. MODY [MIM:606391] is characterized by an autosomal dominant mode of inheritance, onset during young adulthood and a primary defect in insulin secretion.,function:Differentiation factor required for dendrite morphogenesis and maintenance in the cerebellar cortex. Transcriptional activator. Binds to the insulin gene E-box.,PTM:Phosphorylated. In islet cells, phosphorylated on Ser-274 upon glucose stimulation; which may be required for nuclear localization. In activated neurons, phosphorylated on Ser-335; which promotes dendritic growth.,similarity:Contains 1 basic helix-loop-helix (bHLH) domain.,subunit:Efficient DNA binding requires dimerization with another bHLH protein. Heterodimer with TCF3/E47. Interacts with RREB1.,
Subcellular locationCytoplasm . Nucleus . In pancreatic islet cells, shuttles to the nucleus in response to glucose stimulation (By similarity). Colocalizes with NR0B2 in the nucleus. .
ExpressionEye,Retina,Rhabdomyosarcoma,

Additional Images

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Western blot analysis of lysates from HeLa cells treated with UV 15', using Neuro D (Phospho-Ser274) Antibody. The lane on the right is blocked with the phospho peptide.
Image 2
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Immunohistochemical analysis of paraffin-embedded human Squamous cell carcinoma of lung. 1, Antibody was diluted at 1:200(4° overnight). 2, Tris-EDTA,pH9.0 was used for antigen retrieval. 3,Secondary antibody was diluted at 1:200(room temperature, 45min).
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: AO-06-ES6360-50
: 10 Produits
Hurry! only 10 items left in stock.

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