KCNK9 antibody (AA 220-270)

Catalog No. ABIN8123888

This Rabbit Polyclonal antibody specifically detects KCNK9 in WB, IHC and IF. It exhibits reactivity toward Human, Rat and Mouse.

Quick Overview for KCNK9 antibody (AA 220-270) (ABIN8123888)

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

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCNK9 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

Product Details anti-KCNK9 Antibody

Binding Specificity: AA 220-270

Purpose: KCNK9 (TASK-3) Antibody

Specificity: KCNK9(TASK-3) protein(A239) detects endogenous levels of KCNK9(TASK-3)

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthetic Peptide of KCNK9 (TASK-3) AA range: 220-270

Isotype: IgG

Application Details

Application Notes: WB 1:1000-2000, IHC 1:100-200. IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

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/1 year

Expiry Date: 12 months

Target Details for KCNK9

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

Alternative Name: KCNK9

Background:

Synonyms: Potassium channel subfamily K member 9 (Acid-sensitive potassium channel protein TASK-3, TWIK-related acid-sensitive K(+) channel 3, Two pore potassium channel KT3.2, Two pore K(+) channel KT3.2)

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. [provided by RefSeq, Sep 2013],

Gene Name: KCNK9

Protein Name: Potassium channel subfamily K member 9 (Acid-sensitive potassium channel protein TASK-3) (TWIK-related acid-sensitive K(+) channel 3) (Two pore potassium channel KT3.2) (Two pore K(+) channel KT3.2)

Gene ID: 51305

UniProt: Q9NPC2