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CLCNKB 抗体 (AA 51-150) (Cy5.5)

This anti-CLCNKB antibody is a 兔 多克隆 antibody detecting CLCNKB in IF (cc) 和 IF (p). Suitable for 人.
产品编号 ABIN1705681
发货至: 中国

Quick Overview for CLCNKB 抗体 (AA 51-150) (Cy5.5) (ABIN1705681)

抗原

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

适用

  • 36
  • 12
  • 5
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  • 2
  • 2
  • 2
  • 1
  • 1

宿主

  • 39

克隆类型

  • 39
多克隆

标记

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  • 1
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  • 1
  • 1
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This CLCNKB antibody is conjugated to Cy5.5

应用范围

  • 21
  • 19
  • 12
  • 12
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 7
    • 7
    • 6
    • 5
    • 2
    AA 51-150

    预测反应

    Human,Mouse,Rat,Dog,Cow,Pig,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human CLCNKB

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

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

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    CLCNKB (Chloride Channel Kb (CLCNKB))

    别名

    CLCNKB

    背景

    Synonyms: Bartter syndrome type 3, Chloride channel Kb, Chloride channel kidney B, Chloride channel protein ClC-Kb, Chloride channel voltage sensitive Kb, ClC K2, ClC-K2, ClCK2, CLCKB, CLCKB_HUMAN, CLCNKB, hClC Kb, hClCKb, MGC24087, OTTHUMP00000011120, OTTHUMP00000011121, RP11 5P18.8.

    Background: 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. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter?s syndrome which is characterized by renal salt-wasting and low blood pressure.

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