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CHN1, Blocking Peptide

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产品名称: CHN1, Blocking Peptide
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简单介绍

CHN1, Blocking Peptide


CHN1, Blocking Peptide  的详细介绍
Product Name

CHN1, Blocking Peptide

Full Product Name

CHN1 Peptide

Product Gene Name

CHN1 blocking peptide

[Similar Products]
Product Synonym Gene Name
ARHGAP2; CHN; RHOGAP2; NC; DURS2[Similar Products]
Antibody/Peptide Pairs
CHN1 peptide (MBS3235494) is used for blocking the activity of CHN1 antibody (MBS3210539)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
gene 604356
3D Structure
ModBase 3D Structure for P15882
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 CHN1 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
CHN1 blocking peptide
This is a synthetic peptide designed for use in combination with anti-CHN1 antibody made

Target Description: CHN1 contains 1 phorbol-ester/DAG-type zinc finger, 1 Rho-GAP domain and 1 SH2 domain. CHN1 is a GTPase-activating protein for p21-rac and a phorbol ester receptor. It may play an important role in neuronal signal-transduction mechanisms.
Product Categories/Family for CHN1 blocking peptide
Peptide
Applications Tested/Suitable for CHN1 blocking peptide
Western Blot (WB)
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NCBI/Uniprot data below describe general gene information for CHN1. It may not necessarily be applicable to this product.
NCBI GI #
4502813
NCBI GeneID
1123
NCBI Accession #
NP_001813 [Other Products]
NCBI GenBank Nucleotide #
NM_001822 [Other Products]
UniProt Primary Accession #
P15882 [Other Products]
UniProt Related Accession #
P15882[Other Products]
Molecular Weight
53kDa
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NCBI Official Full Name
N-chimaerin isoform 1
NCBI Official Synonym Full Names
chimerin 1
NCBI Official Symbol
CHN1  [Similar Products]
NCBI Official Synonym Symbols
NC; CHN; DURS2; ARHGAP2; RHOGAP2
  [Similar Products]
NCBI Protein Information
N-chimaerin
UniProt Protein Name
N-chimaerin
UniProt Synonym Protein Names
A-chimaerin; Alpha-chimerin; N-chimerin; NC; Rho GTPase-activating protein 2
Protein Family
N-chimaerin
UniProt Gene Name
CHN1  [Similar Products]
UniProt Synonym Gene Names
ARHGAP2; CHN; NC  [Similar Products]
UniProt Entry Name
CHIN_HUMAN
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NCBI Summary for CHN1
This gene encodes GTPase-activating protein for ras-related p21-rac and a phorbol ester receptor. It is predominantly expressed in neurons, and plays an important role in neuronal signal-transduction mechanisms. Mutations in this gene are associated with Duane's retraction syndrome 2 (DURS2). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Apr 2011]
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UniProt Comments for CHN1
ARHGAP2: GTPase-activating protein for p21-rac and a phorbol ester receptor. Involved in the assembly of neuronal locomotor circuits as a direct effector of EPHA4 in axon guidance. Interacts with EPHA4; effector of EPHA4 in axon guidance linking EPHA4 activation to RAC1 regulation. In neurons in brain regions that are involved in learning and memory processes. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: GAPs; Adaptor/scaffold; GAPs, Rac/Rho

Chromosomal Location of Human Ortholog: 2q31.1

Cellular Component: cytosol

Molecular Function: SH3/SH2 adaptor activity; ephrin receptor binding; metal ion binding; GTPase activator activity

Biological Process: regulation of small GTPase mediated signal transduction; positive regulation of signal transduction; small GTPase mediated signal transduction; ephrin receptor signaling pathway; motor axon guidance; regulation of axonogenesis; positive regulation of GTPase activity

Disease: Duane Retraction Syndrome 2
Research Articles on CHN1
1. CHN1 mutations were identified in 2 bilateral cases and in 1 parent of 1 affected case. One mutation is novel and occurred with additional vertical gaze abnormalities.
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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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