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          • Primary Antibodies ›
          • CLCN7 Antibodies

          Osenses

          CLCN7 Polyclonal Antibody

          2 References
          View all (5) CLCN7 antibodies

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          Cite CLCN7 Polyclonal Antibody

          Additional Information:
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          CLCN7 Polyclonal Antibody

          Product Details

          OSC00148W-100UL

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:300-1:2,000
          -

          Immunohistochemistry (IHC)

          1:300-1:2,000
          -

          Miscellaneous PubMed (Misc)

          -
          View 2 publications 2 publications
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Rabbit / Ig

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          A synthetic peptide from aa region 250-300 of human CLCN7 conjugated to blue carrier protein was used as the antigen
          3D Epitope / Immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Lyophilized

          Concentration

          Conc. 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 added 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 of this antibody: 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 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.

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

          Bioinformatics

          Protein Aliases: Chloride channel 7 alpha subunit; Chloride channel protein 7; chloride channel, voltage-sensitive 7; CLC-7; CLCN-7; H(+)/Cl(-) exchange transporter 7; protein phosphatase 1, regulatory subunit 63; unnamed protein product

          View more View less

          Gene Aliases: AA409691; AW538136; CLC-7; CLC7; CLCN7; D17Wsu51e; HOD; OPTA2; OPTB4; PPP1R63

          View more View less

          UniProt ID: (Human) P51798, (Rat) P51799, (Mouse) O70496

          View more View less

          Entrez Gene ID: (Human) 1186, (Rat) 29233, (Mouse) 26373

          View more View less

          Function(s)
          nucleotide binding chloride channel activity protein binding ATP binding chloride transmembrane transporter activity antiporter activity chloride:proton antiporter activity molecular_function voltage-gated chloride channel activity ion channel activity ion channel
          Process(es)
          ion transport chloride transport response to pH transepithelial chloride transport transmembrane transport chloride transmembrane transport hydrogen ion transmembrane transport ion transmembrane transport regulation of anion transport transport
          It has to be done as per old AB suggested Products section.

          Disclaimer

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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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