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KCNK9 antibody (AA 1-100)

The Rabbit Polyclonal anti-KCNK9 antibody (ABIN6142757) specifically detects KCNK9 in WB. The antibody is reactive with Human samples.
Catalog No. ABIN6142757
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Quick Overview for KCNK9 antibody (AA 1-100) (ABIN6142757)

Target

See all KCNK9 Antibodies
KCNK9 (Potassium Channel, Subfamily K, Member 9 (KCNK9))

Reactivity

  • 44
  • 5
  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 43
  • 2
Rabbit

Clonality

  • 43
  • 2
Polyclonal

Conjugate

  • 14
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KCNK9 antibody is un-conjugated

Application

  • 33
  • 15
  • 15
  • 8
  • 6
  • 4
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-100

    Sequence

    MKRQNVRTLS LIVCTFTYLL VGAAVFDALE SDHEMREEEK LKAEEIRIKG KYNISSEDYR QLELVILQSE PHRAGVQWKF AGSFYFAITV ITTIGYGHAA

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    A synthetic peptide corresponding to a sequence within amino acids 1-100 of human KCNK9 (NP_001269463.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    KCNK9 (Potassium Channel, Subfamily K, Member 9 (KCNK9))

    Alternative Name

    KCNK9

    Background

    This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH -dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel mental retardation dysmorphism syndrome. Alternative splicing results in multiple transcript variants.,KCNK9,K2p9.1,KT3.2,TASK-3,TASK3,Cancer,Neuroscience,KCNK9

    Molecular Weight

    42 kDa

    Gene ID

    51305

    UniProt

    Q9NPC2
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