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chloride channel 7, ELISA Kit

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产品名称: chloride channel 7, ELISA Kit
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简单介绍

chloride channel 7, ELISA Kit


chloride channel 7, ELISA Kit  的详细介绍
Product Name

chloride channel 7 (CLCN7), ELISA Kit

Full Product Name

Rat H (+) /Cl (-) exchange transporter 7, CLCN7 ELISA Kit

Product Synonym Names
Rat H (+) /Cl (-) exchange transporter 7 (CLCN7) ELISA kit; CLC-7; CLC7; FLJ26686; FLJ39644; FLJ46423; OPTA2; OPTB4; ; chloride channel 7
Product Gene Name

CLCN7 elisa kit

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Request for Current Manual Insert
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3D Structure
ModBase 3D Structure for P51799
Species Reactivity
Rat
Preparation and Storage
Store all reagents at 2-8 degree C
Product Note
Select online data sheet information is drawn from bioinformatics databases, occasionally resulting in ambiguous or non-relevant product information. It is the responsibility of the customer to review, verify, and evaluate the information to make sure it matches their requirements before purchasing the kit. Our ELISA Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of CLCN7 elisa kit 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.
Searchable Terms for CLCN7 purchase
MBS9331722 is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit for analyzing the presence of the chloride channel 7 (CLCN7) ELISA Kit target analytes in biological samples. The concentration gradients of the kit standards or positive controls render a theoretical kit detection range in biological research samples containing CLCN7. The ELISA analytical biochemical technique of the MBS9331722 kit is based on CLCN7 antibody-CLCN7 antigen interactions (immunosorbency) and an HRP colorimetric detection system to detect CLCN7 antigen targets in samples. The ELISA Kit is designed to detect native, not recombinant, CLCN7. Appropriate sample types may include undiluted body fluids and/or tissue homogenates, secretions. Quality control assays assessing reproducibility identified the intra-assay CV (%) and inter-assay CV(%).
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NCBI/Uniprot data below describe general gene information for CLCN7. It may not necessarily be applicable to this product.
NCBI GI #
13928770
NCBI GeneID
29233
NCBI Accession #
NP_113756.1 [Other Products]
NCBI GenBank Nucleotide #
NM_031568.2 [Other Products]
UniProt Primary Accession #
P51799 [Other Products]
UniProt Related Accession #
P51799[Other Products]
Molecular Weight
88,731 Da
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NCBI Official Full Name
H(+)/Cl(-) exchange transporter 7
NCBI Official Synonym Full Names
chloride channel, voltage-sensitive 7
NCBI Official Symbol
Clcn7  [Similar Products]
NCBI Official Synonym Symbols
ClC-7
  [Similar Products]
NCBI Protein Information
H(+)/Cl(-) exchange transporter 7; H(+)/Cl(-) exchange transporter 7; chloride channel protein 7; chloride channel 7 alpha subunit
UniProt Protein Name
H(+)/Cl(-) exchange transporter 7
UniProt Synonym Protein Names
Chloride channel 7 alpha subunit; Chloride channel protein 7; ClC-7
Protein Family
H(+)/Cl(-) exchange transporter
UniProt Gene Name
Clcn7  [Similar Products]
UniProt Synonym Gene Names
ClC-7  [Similar Products]
UniProt Entry Name
CLCN7_RAT
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NCBI Summary for CLCN7
putative voltage-gated chloride channel; mutation in human and mouse homologs is associated with osteopetrosis and retinal degeneration [RGD, Feb 2006]
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UniProt Comments for CLCN7
CLCN7: Slowly voltage-gated channel mediating the exchange of chloride ions against protons. Functions as antiporter and contributes to the acidification of the lysosome lumen. Defects in CLCN7 are the cause of osteopetrosis autosomal recessive type 4 (OPTB4); also known as infantile malignant osteopetrosis type 2. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or *****hood. Defects in CLCN7 are the cause of osteopetrosis autosomal dominant type 2 (OPTA2); also known as autosomal dominant Albers-Schonberg disease or marble disease autosomal dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or *****hood. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or *****hood. It is characterized by sclerosis, predominantly involving the spine, the pelvis and the skull base. Belongs to the chloride channel (TC 2.A.49) family. ClC-7/CLCN7 subfamily.

Protein type: Membrane protein, multi-pass; Membrane protein, integral; Transporter, ion channel; Channel, chloride; Transporter

Cellular Component: membrane; lysosomal membrane; integral to membrane; cytoplasmic vesicle

Molecular Function: voltage-gated chloride channel activity; ATP binding; antiporter activity

Biological Process: chloride transport; response to pH
Research Articles on CLCN7
1. G213R mutation prevents ClC-7 from being correctly targeted to the lysosomal membrane.
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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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