KCNK9 antibody (AA 1-100)

Catalog No. ABIN6142757

Product Details anti-KCNK9 Antibody

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

Binding Specificity: AA 1-100

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This KCNK9 antibody is un-conjugated

Application: Western Blotting (WB)

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 Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

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 Details for KCNK9

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

Alternative Name: KCNK9 (KCNK9 Products)

Synonyms: Task3 antibody, K2p9.1 antibody, KT3.2 antibody, TASK-3 antibody, TASK3 antibody, KCNK9 antibody, LOC799704 antibody, Kcnk9 antibody, task3 antibody, k2p9.1 antibody, task-3 antibody, kt3.2 antibody, potassium channel, subfamily K, member 9 antibody, potassium two pore domain channel subfamily K member 9 antibody, potassium channel, two pore domain subfamily K, member 9 antibody, potassium channel, two pore domain subfamily K, member 9 L homeolog antibody, Kcnk9 antibody, KCNK9 antibody, kcnk9 antibody, kcnk9.L antibody

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