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CLCNKB antibody

The Rabbit Polyclonal anti-CLCNKB antibody has been validated for ELISA and WB. It is suitable to detect CLCNKB in samples from Human.
Catalog No. ABIN7227932

Quick Overview for CLCNKB antibody (ABIN7227932)

Target

See all CLCNKB Antibodies
CLCNKB (Chloride Channel Kb (CLCNKB))

Reactivity

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  • 1
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Human

Host

  • 39
Rabbit

Clonality

  • 39
Polyclonal

Conjugate

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  • 1
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  • 1
  • 1
  • 1
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This CLCNKB antibody is un-conjugated

Application

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ELISA, Western Blotting (WB)
  • Purpose

    CLCKB Polyclonal Antibody

    Specificity

    The antibody detects endogenous levels of CLCKB protein

    Purification

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    Immunogen

    Synthesized peptide derived from part region of human CLCKB protein

    Isotype

    IgG
  • Application Notes

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    Comment

    Primary Antibody

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • Target

    CLCNKB (Chloride Channel Kb (CLCNKB))

    Alternative Name

    CLCKB

    Background

    Rabbit Anti-CLCKB Polyclonal Antibody,Chloride channel protein ClC-Kb, Chloride channel Kb, ClC-K2,CLCNKB (Chloride Voltage-Gated Channel Kb) is a Protein Coding gene. Diseases associated with CLCNKB include Bartter Syndrome, Type 3 and Bartter Syndrome, Type 4B, Digenic. Among its related pathways are Hepatic ABC Transporters and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds.,CLCKB

    Molecular Weight

    observerd band 75kDa

    Gene ID

    1188

    UniProt

    P51801
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