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KCNJ1 antibody (AA 301-391) (Alexa Fluor 647)

KCNJ1 Reactivity: Rat IF (cc), IF (p), FACS Host: Rabbit Polyclonal Alexa Fluor 647
Catalog No. ABIN913907
  • Target See all KCNJ1 Antibodies
    KCNJ1 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 1 (KCNJ1))
    Binding Specificity
    • 19
    • 15
    • 8
    • 8
    • 6
    • 5
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 301-391
    Reactivity
    • 55
    • 24
    • 9
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Rat
    Host
    • 69
    • 1
    • 1
    Rabbit
    Clonality
    • 71
    Polyclonal
    Conjugate
    • 22
    • 9
    • 7
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    This KCNJ1 antibody is conjugated to Alexa Fluor 647
    Application
    • 38
    • 26
    • 25
    • 25
    • 13
    • 10
    • 9
    • 8
    • 6
    • 2
    • 1
    • 1
    Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Flow Cytometry (FACS)
    Cross-Reactivity
    Rat
    Predicted Reactivity
    Human,Mouse,Dog,Cow,Pig,Horse,Rabbit
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human ROM-K/KCNJ1
    Isotype
    IgG
    Top Product
    Discover our top product KCNJ1 Primary Antibody
  • Application Notes
    FCM 1:20-100
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    Expiry Date
    12 months
  • Target
    KCNJ1 (Potassium Inwardly-Rectifying Channel, Subfamily J, Member 1 (KCNJ1))
    Alternative Name
    ROM-K (KCNJ1 Products)
    Synonyms
    KIR1.1 antibody, ROMK antibody, ROMK1 antibody, kir1.1 antibody, romk1 antibody, Kcnj antibody, Kir1.1 antibody, Romk2 antibody, kcnj1 antibody, wu:fl37c05 antibody, zgc:63534 antibody, potassium voltage-gated channel subfamily J member 1 antibody, potassium voltage-gated channel subfamily J member 1 L homeolog antibody, potassium inwardly-rectifying channel, subfamily J, member 1 antibody, potassium inwardly-rectifying channel, subfamily J, member 1a, tandem duplicate 1 antibody, KCNJ1 antibody, kcnj1.L antibody, kcnj1 antibody, Kcnj1 antibody, kcnj1a.1 antibody
    Background

    Synonyms: ROM K, ROM-K, inwardly rectying subfamily J member 1, ATP regulated potassium channel ROM K, ATP sensitive inward rectier potassium channel 1, ATP-regulated potassium channel ROM-K, ATP-sensitive inward rectier potassium channel 1, Inward rectier K+ channel Kir1.1, inwardly rectying K+ channel, IRK1_HUMAN, KCNJ 1, KCNJ, Kcnj1, Kir 1.1, Kir1.1, Potassium channel, Potassium channel inwardly rectying subfamily J member 1, potassium inwardly-rectying channel J1, ROMK 1, ROMK 2, ROMK, ROMK1, ROMK2.

    Background: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. It is activated by internal ATP and probably plays an important role in potassium homeostasis. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Mutations in this gene have been associated with antenatal Bartter syndrome, which is characterized by salt wasting, hypokalemic alkalosis, hypercalciuria, and low blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].

    Gene ID
    3758
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