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Anti-CLCN5 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Anti-CLCN5 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Catalog # BOSSBS-10307R-HRP
Supplier:  Bioss
Anti-CLCN5 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Catalog # BOSSBS-10307R-HRP
Supplier:  Bioss

Specifications

  • Antibody type:
    Primary
  • Antigen name:
    Chloride Channel 5
  • Antigen symbol:
    CLCN5
  • Clonality:
    Polyclonal
  • Conjugation:
    HRP (Horseradish Peroxidase)
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Western blot:
    Yes
  • Environmentally Preferable:
  • Cross adsorption:
    No
  • Form:
    liquid
  • Antigen synonyms:
    H+/Cl- exchange transporter 5|NPHL2|CLC5|Chloride channel protein 5|CLCN5_HUMAN|DENTS|hCIC-K2|NPHL1|XRN.|XLRH|Chloride transporter ClC-5|CLCK2|ClC-5|CLCN5
  • Storage buffer:
    Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0.09% Gentamicin. Store at 4°C for 12 months.
  • Storage temperature:
    Store at 4°C for 12 months
  • Concentration:
    1 μg/μl
  • Shipping temperature:
    4°C
  • Purification:
    Purified by Protein A
  • Pk:
    100 µl

Specifications

About this item

The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterized by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent’s disease, a renal disorder characterized by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.

Recommended Dilutions: Western Blot: 1:100-1000; IHC-P: 1:100-500

Type: Primary
Antigen: CLCN5
Clonality: Polyclonal
Clone:
Conjugation: HRP (Horseradish Peroxidase)
Epitope:
Host: Rabbit
Isotype:
Reactivity: