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Anti-CLCNKB Antibody (C-Terminus) LS-C144769

Ordering

Wt. Vol. Conc. Price
- 100 µl - Unavailable

Related Products

21 CLCNKB Antibodies

Most Popular CLCNKB Antibodies

Anti-CLCNKB Antibody (C-Terminus) LS-C19194
Rabbit Polyclonal (IgG) to Human CLCNKB
Human, Monkey, Rat, Bovine, Dog
Western blot
Unconjugated
Western blot Image
Anti-CLCNKB Antibody (N-Terminus) LS-C19293
Rabbit Polyclonal (IgG) to Human CLCNKB
Human, Dog
Western blot
Unconjugated
Western blot Image
Anti-CLCNKB Antibody (C-Terminus) LS-C144769
Rabbit Polyclonal to Mouse CLCNKB
Mouse
IHC, Western blot
Unconjugated
Anti-CLCNKB Antibody (aa11-40) LS-C168807
Rabbit Polyclonal to Human CLCNKB
Human, Mouse
Western blot
Unconjugated
Western blot Image
Anti-CLCNKB Antibody (N-Terminus, Biotin) LS-C432025
Rabbit Polyclonal (IgG) to Human CLCNKB
Human, Chimpanzee, Dog
Western blot
Biotin Conjugated
Western blot Image

100% Guaranteed 100% Guaranteed
Rabbit Polyclonal to Mouse CLCNKB
Mouse
IHC, Western blot
Unconjugated

Details

Mouse CLCNKB
Rabbit
Mouse (tested or 100% immunogen sequence identity)
Polyclonal
Unconjugated
Antiserum
Unmodified

Applications

  • IHC (1:200 - 1:1000)
  • Western blot (1:500 - 1:5000)

Specificity and Use

CLCNKB antibody was raised against synthetic peptide derived from Cter domain of ClC-Kb protein
C-Terminus
Mouse 75 kD protein

Packaging

Lyophilized antiserum
100 µl Distilled water
Long term: -20°C; Short term: +4°C. Avoid repeat freeze-thaw cycles.
For research use only.

About CLCNKB

P51801 NM_000085 NP_000076.2

CLCNKB Antibody, Bartter syndrome Type 3 Antibody, Chloride channel, kidney, B Antibody, Chloride channel Kb Antibody, ClC-Kb Antibody, ClC-K2 Antibody, CLCKB Antibody, HClC-Kb Antibody

CLCNKB is a member of the family of voltage-gated chloride channels. Chloride channels have several functions, including the regulation of cell volume, membrane potential stabilization, signal transduction and transepithelial transport. This gene is expressed predominantly in the kidney and may be important for renal salt reabsorption. Mutations in this gene are associated with autosomal recessive Bartter syndrome type 3 (BS3).

Requested From: 
Date Requested: 4/23/2017

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