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ELK Biotechnology KIR6.2 (phospho Thr224) rabbit pAb
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ELK Biotechnology KIR6.2 (phospho Thr224) rabbit pAb

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KIR6.2 (phospho Thr224) rabbit polyclonal antibody로, 인산화 Thr224 부위를 인식합니다. WB, IHC, IF, ELISA에 적합하며, 인간, 마우스, 랫트 시료에 반응합니다. 막 단백질 연구 및 당뇨 관련 단백질 분석에 유용합니다.

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pk
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ELK Biotechnology ES6009-100UL KIR6.2 (phospho Thr224) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES6009-50UL KIR6.2 (phospho Thr224) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology KIR6.2 (phospho Thr224) rabbit pAb

제품명

KIR6.2 (phospho Thr224) rabbit pAb

제품 개요

본 항체는 인간 Kir6.2 단백질의 Thr224 인산화 부위를 인식하도록 합성된 펩타이드로부터 제작된 rabbit polyclonal antibody입니다. Kir6.2는 ATP-sensitive inward rectifier potassium channel로, 세포막을 통한 칼륨 이온 이동 조절에 관여합니다.

제품 정보

항목 내용
Product Name KIR6.2 (phospho Thr224) rabbit pAb
Alternative Names KCNJ11; ATP-sensitive inward rectifier potassium channel 11; IKATP; Inward rectifier K(+) channel Kir6.2; Potassium channel; inwardly rectifying subfamily J member 11
Applications WB; IHC; IF; ELISA
Recommended Dilutions WB: 1/500–1/2000
IHC: 1/100–1/300
IF: 1/200–1/1000
ELISA: 1/5000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human Kir6.2 around phosphorylation site Thr224 (AA 190–239)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 40 kDa
Gene ID (Human) 3767
Human Swiss-Prot No. Q14654
Cellular Localization Membrane; Multi-pass membrane protein
Species Reactivity Human; Mouse; Rat

Background

Potassium channels are present in most mammalian cells and participate in various physiological responses. The Kir6.2 protein is an inward-rectifier potassium channel controlled by G-proteins and associated with the sulfonylurea receptor SUR. Mutations in this gene can cause familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI) and may contribute to disorders such as type II diabetes mellitus (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcripts have been identified.

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