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CLCNKA antibody (C-Term, Intracellular)

This Rabbit Polyclonal antibody specifically detects CLCNKA in WB, IHC and IF. It exhibits reactivity toward Mouse and Rat.
Catalog No. ABIN7884876
$1,466.46
Plus shipping costs $50.00
200 μL
Shipping to: United States
Delivery in 11 to 14 Business Days

Quick Overview for CLCNKA antibody (C-Term, Intracellular) (ABIN7884876)

Target

See all CLCNKA Antibodies
CLCNKA (Chloride Channel Ka (CLCNKA))

Reactivity

  • 28
  • 5
  • 4
  • 1
  • 1
Mouse, Rat

Host

  • 29
Rabbit

Clonality

  • 29
Polyclonal

Conjugate

  • 17
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This CLCNKA antibody is un-conjugated

Application

  • 22
  • 12
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Grade

Carrier-free
  • Binding Specificity

    • 9
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 674-687, C-Term, Intracellular

    Purpose

    A Rabbit Polyclonal Antibody to CLC-K Channel

    Predicted Reactivity

    Mouse - identical, human - 13,14 amino acid residues identical

    Purification

    Affinity purified on immobilized antigen.

    Immunogen

    (C)KKAISTLTNPPAPK, corresponding to amino acid residues 674-687 of the rat longer form CLC-K2L

    Isotype

    IgG
  • Application Notes

    WB: 1:200

    FC: The optimal concentration should be determined by the user

    ICC: The optimal concentration should be determined by the user

    IHC: The optimal concentration should be determined by the user

    IP: The optimal concentration should be determined by the user

    Comment

    Negative Control: (ABIN7235094)

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    0.2 mL double distilled water (DDW)

    Concentration

    1 mg/mL

    Buffer

    PBS pH 7.4

    Preservative

    Without preservative

    Storage

    -20 °C

    Storage Comment

    The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C
  • Target

    CLCNKA (Chloride Channel Ka (CLCNKA))

    Alternative Name

    CLC-K1

    Background

    Synonyms: CLC-K1, CLC-K2, CLC-Ka, CLC-Kb, Clcnka, Clcnkb, ClCk, Chloride channel K

    Description: CLC-Ka and CLC-Kb are members of the voltage-dependent Cl- channel (CLC) family that includes nine known members in mammals. The human CLC-Ka and CLC-Kb (known as CLC-K1 and CLC-K2 in the rat) channels are closely related genes that share 94 % sequence homology and identical genomic organization.CLC channels can be classified as plasma membrane channels and intracellular organelle channels. The first group includes the CLC-1, CLC-2, CLC-Ka and CLC-Kb channels. The second group comprises the CLC-3, CLC-4, CLC-5, CLC-6 and CLC-7.CLC channels that function in the plasma membrane are involved in the stabilization of membrane potential and in transepithelial transport. The presumed function of the intracellular CLC channels is support of the acidification of the intraorganellar compartment. In this regard, recent reports indicate that CLC-4 and CLC-5 (and by inference CLC-3) can function as Cl-/H+ antiporters.1, 2The functional unit of the CLC channels is a dimer with each subunit forming a proper pore. Although the crystal structure of bacterial CLC channels was resolved,the topology of the CLC channels is complex and has not been fully elucidated. It is generally accepted that both the N- and C- terminus domains are intracellular while the number and configuration of the transmembrane domains vary greatly between different models. 1,2CLC-K channels require the presence of the auxiliary b subunit barttin, a 34 kD transmembrane protein, for transport to the plama membrane and regulation of channel permeation and gating.3CLC-K channels are expressed primarily in the kidney from the thin ascending limb to the collecting duct of the nephron, and in the stria vascularis and dark cells of the vestibular organ of the inner ear.The channels are important for renal salt reabsorption and water balance by enabling chloride exit across the basolateral membranes. The importance of the CLC-K channel in renal function is demonstrated by the fact that loss-of-function mutations in CLC-Kb lead to Bartter syndrome type III, an autosomal recessive disorder characterized by severe salt wasting, low blood pressure, hypokalemia and hypercalciuria.4

    Gene ID

    79430

    UniProt

    P51802

    Pathways

    Response to Water Deprivation
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