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CLCNKB Antikörper (AA 51-150) (AbBy Fluor® 350)

CLCNKB Reaktivität: Human IF (cc), IF (p) Wirt: Kaninchen Polyclonal AbBy Fluor® 350
Produktnummer ABIN1692979
  • Target Alle CLCNKB Antikörper anzeigen
    CLCNKB (Chloride Channel Kb (CLCNKB))
    Bindungsspezifität
    • 14
    • 11
    • 7
    • 7
    • 6
    • 6
    • 1
    • 1
    AA 51-150
    Reaktivität
    • 41
    • 18
    • 6
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Human
    Wirt
    • 50
    Kaninchen
    Klonalität
    • 50
    Polyklonal
    Konjugat
    • 17
    • 5
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser CLCNKB Antikörper ist konjugiert mit AbBy Fluor® 350
    Applikation
    • 26
    • 23
    • 12
    • 12
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    Homologie
    Human,Mouse,Rat,Dog,Cow,Pig,Rabbit
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human CLCNKB
    Isotyp
    IgG
    Top Product
    Discover our top product CLCNKB Primärantikörper
  • Applikationshinweise
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Haltbarkeit
    12 months
  • Target
    CLCNKB (Chloride Channel Kb (CLCNKB))
    Andere Bezeichnung
    CLCNKB (CLCNKB Produkte)
    Synonyme
    CLCNKA antikoerper, CLCNKB antikoerper, DKFZp469N0132 antikoerper, CLCKB antikoerper, Clc-Ka antikoerper, Clck2 antikoerper, Clcnk1l antikoerper, ClC-K2L antikoerper, ClC-K2 antikoerper, ClC-Kb antikoerper, ClC-k antikoerper, clc-kb antikoerper, clckb antikoerper, clcnka-A antikoerper, clk-k2 antikoerper, x6clck antikoerper, xCIC-K antikoerper, xClC-K antikoerper, zgc:64141 antikoerper, Clcnkb antikoerper, chloride voltage-gated channel Kb antikoerper, chloride channel Kb antikoerper, chloride channel, voltage-sensitive Kb antikoerper, chloride channel, voltage-sensitive Kb L homeolog antikoerper, chloride channel K antikoerper, chloride channel protein ClC-Ka antikoerper, chloride channel protein ClC-Kb antikoerper, CLCNKB antikoerper, Clcnkb antikoerper, clcnkb.L antikoerper, clcnk antikoerper, LOC100017912 antikoerper, LOC100400180 antikoerper, LOC100590605 antikoerper, LOC100730738 antikoerper
    Hintergrund

    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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