Human IgG antibody Laboratories manufactures the proteintech neurod1 rabbit polyclonal antibody reagents distributed by Genprice. The Proteintech Neurod1 Rabbit Polyclonal Antibody reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact rabbit polyclonal. Other Proteintech products are available in stock. Specificity: Proteintech Category: Neurod1 Group: Rabbit Polyclonal
NeuroD1 Antibody |
SAB |
50ul |
EUR 286.8 |
NEUROD1 antibody |
Fitzgerald |
50 ul |
EUR 522 |
Description: Rabbit polyclonal NEUROD1 antibody |
NEUROD1 Antibody |
Cusabio |
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|
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Description: A polyclonal antibody against NEUROD1. Recognizes NEUROD1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC |
NEUROD1 Antibody |
Cusabio |
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|
|
Description: A polyclonal antibody against NEUROD1. Recognizes NEUROD1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/5000 |
NEUROD1 Antibody |
Cusabio |
|
|
|
Description: A polyclonal antibody against NEUROD1. Recognizes NEUROD1 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IF; Recommended dilution: WB:1:200-1:2000, IF:1:50-1:200 |
NeuroD1 Antibody |
NSJ Bioreagents |
0.08 ml |
EUR 140.25 |
Description: NeuroD1 acts as a differentiation factor during neurogenesis. They are expressed transiently in a subset of neurons in the central and peripheral nervous systems at the time of their terminal differentiation. NeuroD1 is a basic helix-loop-helix (bHLH) protein contain 1 bHLH domain. NeuroD1 is a transcriptional activator, for efficient DNA binding it requires dimerization with another bHLH protein. It was reported that NeuroD1 involves heterodimerization with the ubiquitous bHLH protein E47, and regulates insulin gene expression by binding to a critical E-box motif on the insulin promoter. Defects in NEUROD1 causes maturity onset diabetes of the young type VI. MODY6 is a form of non-insulin-dependent diabetes mellitus (NIDDM) characterized by an autosomal dominant mode of inheritance, onset during young adulthood and a primary defect in insulin secretion. |
Rabbit Polyclonal information
Polyclonal NEUROD2 Antibody (C-Term) |
AMM06626G |
Leading Biology |
0.1 mg |
EUR 580.8 |
Description: A polyclonal antibody raised in Goat that recognizes and binds to Human NEUROD2 (C-Term). This antibody is tested and proven to work in the following applications: |
NeuroD1 (C-term) Rabbit pAb |
E2614571 |
EnoGene |
100ul |
EUR 225 |
Description: Available in various conjugation types. |
Polyclonal NEUROD4 antibody - middle region |
AMM06628G |
Leading Biology |
0.05mg |
EUR 633.6 |
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human NEUROD4 - middle region. This antibody is tested and proven to work in the following applications: |
Polyclonal Neuro-d4 / DPF1 Antibody (C-Term) |
AMM06622G |
Leading Biology |
0.1 mg |
EUR 580.8 |
Description: A polyclonal antibody raised in Goat that recognizes and binds to Human Neuro-d4 / DPF1 (C-Term). This antibody is tested and proven to work in the following applications: |
NEUROD1 antibody |
38203-100ul |
SAB |
100ul |
EUR 302.4 |
NeuroD1 Antibody |
49486-100ul |
SAB |
100ul |
EUR 399.6 |
NeuroD1 Antibody |
49486-50ul |
SAB |
50ul |
EUR 286.8 |
NEUROD1 antibody |
70R-18851 |
Fitzgerald |
50 ul |
EUR 522 |
Description: Rabbit polyclonal NEUROD1 antibody |
NEUROD1 Antibody |
1-CSB-PA015725GA01HU |
Cusabio |
|
|
|
Description: A polyclonal antibody against NEUROD1. Recognizes NEUROD1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: ELISA, IHC |
NEUROD1 Antibody |
1-CSB-PA020064 |
Cusabio |
|
|
|
Description: A polyclonal antibody against NEUROD1. Recognizes NEUROD1 from Human, Mouse, Rat. This antibody is Unconjugated. Tested in the following application: WB, ELISA;WB:1/500-1/2000.ELISA:1/5000 |
NEUROD1 Antibody |
1-CSB-PA615700LA01HU |
Cusabio |
|
|
|
Description: A polyclonal antibody against NEUROD1. Recognizes NEUROD1 from Human, Mouse. This antibody is Unconjugated. Tested in the following application: ELISA, WB, IF; Recommended dilution: WB:1:200-1:2000, IF:1:50-1:200 |
NeuroD1 Antibody |
F47842-0.08ML |
NSJ Bioreagents |
0.08 ml |
EUR 140.25 |
Description: NeuroD1 acts as a differentiation factor during neurogenesis. They are expressed transiently in a subset of neurons in the central and peripheral nervous systems at the time of their terminal differentiation. NeuroD1 is a basic helix-loop-helix (bHLH) protein contain 1 bHLH domain. NeuroD1 is a transcriptional activator, for efficient DNA binding it requires dimerization with another bHLH protein. It was reported that NeuroD1 involves heterodimerization with the ubiquitous bHLH protein E47, and regulates insulin gene expression by binding to a critical E-box motif on the insulin promoter. Defects in NEUROD1 causes maturity onset diabetes of the young type VI. MODY6 is a form of non-insulin-dependent diabetes mellitus (NIDDM) characterized by an autosomal dominant mode of inheritance, onset during young adulthood and a primary defect in insulin secretion. |
NeuroD1 Antibody |
F47842-0.4ML |
NSJ Bioreagents |
0.4 ml |
EUR 322.15 |
Description: NeuroD1 acts as a differentiation factor during neurogenesis. They are expressed transiently in a subset of neurons in the central and peripheral nervous systems at the time of their terminal differentiation. NeuroD1 is a basic helix-loop-helix (bHLH) protein contain 1 bHLH domain. NeuroD1 is a transcriptional activator, for efficient DNA binding it requires dimerization with another bHLH protein. It was reported that NeuroD1 involves heterodimerization with the ubiquitous bHLH protein E47, and regulates insulin gene expression by binding to a critical E-box motif on the insulin promoter. Defects in NEUROD1 causes maturity onset diabetes of the young type VI. MODY6 is a form of non-insulin-dependent diabetes mellitus (NIDDM) characterized by an autosomal dominant mode of inheritance, onset during young adulthood and a primary defect in insulin secretion. |