anti-KCNJ11 / Kir6.2 antibody
CAT.NO. : ARG64391
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概述
产品描述 | Goat Polyclonal antibody recognizes KCNJ11 / Kir6.2 |
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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 |
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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 |
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纯化 | Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide. |
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 | Swiss-port # Q14654 Human ATP-sensitive inward rectifier potassium channel 11 |
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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)
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.
