CLCN7 Antibody (RB31756)

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Product Details

Summary
Product Discontinued
View other related CLCN7 Primary Antibodies

Order Details


    • Catalog Number
      NBP2-30021
    • Availability
      Product Discontinued

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CLCN7 Antibody (RB31756) Summary

Immunogen
This CLCN7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 692-720 amino acids from the C-terminal region of human CLCN7.
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
CLCN7
Purity
Protein A purified
Innovator's Reward
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Applications/Dilutions

Dilutions
  • Immunocytochemistry/ Immunofluorescence 1:10 - 1:50
  • Immunohistochemistry 1:10-1:500
  • Immunohistochemistry-Paraffin 1:10 - 1:50
  • Western Blot 1:1000
Theoretical MW
88.679 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Reactivity Notes

Predicted to react with Bovine, Mouse and Rat.

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
PBS
Preservative
0.09% Sodium Azide
Concentration
0.5 mg/ml
Purity
Protein A purified

Alternate Names for CLCN7 Antibody (RB31756)

  • chloride channel 7
  • Chloride channel protein 7
  • CLC-7
  • CLC7FLJ39644
  • FLJ26686
  • H(+)/Cl(-) exchange transporter 7
  • OPTA2FLJ46423
  • OPTB4

Background

The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol
ICC/IF Video Protocol

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Secondary Antibodies

 

Isotype Controls

Additional CLCN7 Products

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Bioinformatics

Gene Symbol CLCN7
Uniprot