ARG64391

anti-KCNJ11 / Kir6.2 antibody

anti-KCNJ11 / Kir6.2 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Cancer antibody; Cell Biology and Cellular Response antibody; Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody

概述

产品描述 Goat Polyclonal antibody recognizes KCNJ11 / Kir6.2
反应物种 Hu
应用 IHC-P, WB
特异性 This antibody is expected to recognise isoform 1 (NP_000516.3) only.
宿主 Goat
克隆 Polyclonal
同位型 IgG
靶点名称 KCNJ11 / Kir6.2
抗原物种 Human
抗原 C-AEDPAKPRYRARQ
偶联标记 Un-conjugated
別名 IKATP; TNDM3; ATP-sensitive inward rectifier potassium channel 11; PHHI; HHF2; KIR6.2; MODY13; Potassium channel, inwardly rectifying subfamily J member 11; Inward rectifier K; BIR

应用说明

应用建议
应用 推荐稀释比
IHC-P3 - 5 µg/ml
WB0.1 - 0.3 µg/ml
应用说明 IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

属性

形式 Liquid
纯化 Purified from goat serum by antigen affinity chromatography.
缓冲液 Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
抗菌剂 0.02% Sodium azide
稳定剂 0.5% BSA
浓度 0.5 mg/ml
存放说明 For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项 For laboratory research only, not for drug, diagnostic or other use.

生物信息

数据库连接

GeneID: 3767 Human KCNJ11

Swiss-port # Q14654 Human ATP-sensitive inward rectifier potassium channel 11

背景介绍 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. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Oct 2009]
研究领域 Cancer antibody; Cell Biology and Cellular Response antibody; Metabolism antibody; Neuroscience antibody; Signaling Transduction antibody
预测分子量 44 kDa
翻译后修饰 Phosphorylation by MAPK1 results in changes in channel gating that destabilize the closed states and reduce the ATP sensitivity.

检测图片 (2) Click the Picture to Zoom In

  • ARG64391 anti-KCNJ11 / Kir6.2 antibody WB image

    Western blot: 35 µg of Human Muscle lysate stained with ARG64391 anti-KCNJ11 / Kir6.2 antibody at 0.1 µg/ml dilution.

  • ARG64391 anti-KCNJ11 / Kir6.2 antibody IHC image

    Immunohistochemistry: paraffin-embedded Human Pancreas (Steamed antigen retrieval with citrate buffer pH 6) stained with ARG64391 anti-KCNJ11 / Kir6.2 antibody at 3.8 µg/ml dilution, followed by AP-staining.