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Thermo Fisher Scientific CLCN7 Polyclonal Antibody
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Thermo Fisher Scientific CLCN7 Polyclonal Antibody

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Rabbit polyclonal antibody targeting human CLCN7, reactive with human, mouse, and rat. Suitable for WB and IHC applications. Lyophilized form with no preservative, ideal for research use. Stable at -20°C with glycerol addition.

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pk
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Thermo Fisher Scientific OSC00148W-100UL CLCN7 Polyclonal Antibody 100 ul pk판매 단위 pk
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Thermo Fisher Scientific · Thermo Fisher Scientific CLCN7 Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:300–1:2,000 -
Immunohistochemistry (IHC) 1:300–1:2,000 -
Miscellaneous PubMed (Misc) - View 2 publications

Product Specifications

Property Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from amino acid region 250–300 of human CLCN7 conjugated to blue carrier protein
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long-term storage, store at -20°C avoiding freeze/thaw cycles. Glycerol (1:1) may be added for stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 100 µL of sterile water.
  • Centrifuge to remove any insoluble material.
  • The antigen is homologous in rat and mouse.
  • Specificity: CLCN7.

Target Information

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


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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