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NDN, Blocking Peptide

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产品名称: NDN, Blocking Peptide
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简单介绍

NDN, Blocking Peptide


NDN, Blocking Peptide  的详细介绍
Product Name

NDN, Blocking Peptide

Full Product Name

NDN Peptide - middle region

Product Gene Name

NDN blocking peptide

[Similar Products]
Product Synonym Gene Name
HsT16328; PWCR[Similar Products]
Antibody/Peptide Pairs
NDN peptide (MBS3237673) is used for blocking the activity of NDN antibody (MBS3212726)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
phenotype 602117
3D Structure
ModBase 3D Structure for Q99608
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of NDN blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
NDN blocking peptide
This is a synthetic peptide designed for use in combination with anti-NDN antibody made

Target Description: This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic
Product Categories/Family for NDN blocking peptide
Peptide
Applications Tested/Suitable for NDN blocking peptide
Western Blot (WB)
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NCBI/Uniprot data below describe general gene information for NDN. It may not necessarily be applicable to this product.
NCBI GI #
4505349
NCBI GeneID
4692
NCBI Accession #
NP_002478 [Other Products]
NCBI GenBank Nucleotide #
NM_002487 [Other Products]
UniProt Primary Accession #
Q99608 [Other Products]
UniProt Related Accession #
Q99608[Other Products]
Molecular Weight
36kDa
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NCBI Official Full Name
necdin
NCBI Official Synonym Full Names
necdin, MAGE family member
NCBI Official Symbol
NDN  [Similar Products]
NCBI Official Synonym Symbols
PWCR; HsT16328
  [Similar Products]
NCBI Protein Information
necdin
UniProt Protein Name
Necdin
Protein Family
Necdin
UniProt Gene Name
NDN  [Similar Products]
UniProt Entry Name
NECD_HUMAN
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NCBI Summary for NDN
This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons. [provided by RefSeq, Jul 2008]
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UniProt Comments for NDN
NDN: Growth suppressor that facilitates the entry of the cell into cell cycle arrest. Functionally similar to the retinoblastoma protein it binds to and represses the activity of cell-cycle- promoting proteins such as SV40 large T antigen, adenovirus E1A, and the transcription factor E2F. Necdin also interacts with p53 and works in an additive manner to inhibit cell growth. Functions also as transcription factor and binds directly to specific guanosine-rich DNA sequences.

Protein type: Transcription factor; DNA-binding

Chromosomal Location of Human Ortholog: 15q11.2-q12

Cellular Component: centrosome; cell projection; perikaryon; cytosol; nucleus

Molecular Function: gamma-tubulin binding; DNA binding

Biological Process: nervous system development; central nervous system development; transcription, DNA-dependent; nerve growth factor receptor signaling pathway; axon extension; neuron migration; axonal fasciculation; multicellular organismal homeostasis; glial cell migration; sensory perception of pain; post-embryonic development; respiratory system process; negative regulation of cell proliferation; regulation of transcription, DNA-dependent; regulation of growth

Disease: Prader-willi Syndrome
Research Articles on NDN
1. the single-nucleotide polymorphism rs850807, which is putatively functional and linked with MAGEL2 and NDN Genetic variation in rs850807 was strongly and exclusively associated with the ideas of reference subscale of the schizophrenia spectrum, which is best typified as paranoia
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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