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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 recognizing human CLCN7 protein. Validated for IHC and ICC/IF. Antigen affinity purified, supplied in PBS with glycerol. Suitable for research on chloride channel function and osteopetrosis-related studies.

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마지막 업데이트 2025. 08. 04. 오전 01:20
Thermo Fisher Scientific PA560426 CLCN7 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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876,300원VAT 포함 963,930원

Thermo Fisher Scientific · Thermo Fisher Scientific CLCN7 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC-P) 1:20–1:50
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human CLCN7. Recombinant protein control fragment (Product #RP-98666).
Conjugate Unconjugated
Form Liquid
Concentration 0.05 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2639860

Product Specific Information

Immunogen sequence:
LRLKDFRDAY PRFPPIQSIH VSQDERECTM DLSEFMNPSP YTVPQEASLP RVFKLFRALG LRHLVVVDNR NQVVGLVT

Highest antigen sequence identity:

  • Mouse: 99%
  • Rat: 99%

Target Information

The CLCN7 gene encodes chloride channel 7, a member of the CLC chloride channel family. These channels are essential for chloride ion transport across plasma membranes and within intracellular organelles. Mutations in CLCN7 are associated with osteopetrosis autosomal recessive type 4 (OPTB4), also known as infantile malignant osteopetrosis type 2, and with autosomal dominant osteopetrosis type 2 (OPTA2), also called Albers-Schonberg disease or marble disease. Osteopetrosis is a rare genetic disorder characterized by abnormally dense bone due to defective bone resorption. OPTA2 typically manifests during adolescence or adulthood.


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

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