CLIC2 抗体 (AA 51-150) (Biotin)
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- 抗原 See all CLIC2 抗体
- CLIC2 (Chloride Intracellular Channel 2 (CLIC2))
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抗原表位
- AA 51-150
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This CLIC2 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Rat,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CLIC2
- 亚型
- IgG
- Top Product
- Discover our top product CLIC2 Primary Antibody
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- 应用备注
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IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- CLIC2 (Chloride Intracellular Channel 2 (CLIC2))
- 别名
- CLIC2 (CLIC2 产品)
- 别名
- zgc:92762 antibody, CLIC2 antibody, CLIC2b antibody, MRXS32 antibody, XAP121 antibody, chloride intracellular channel 2 antibody, clic2 antibody, CLIC2 antibody, Clic2 antibody
- 背景
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Synonyms: Chloride intracellular channel 2, Chloride intracellular channel protein 2, CLIC 2b, CLIC2, CLIC2_HUMAN, CLIC2b, MRXS32, OTTHUMP00000196471, XAP 121, XAP121.
Background: Chloride channels (CLCs) regulate cellular traffic of chloride ions, a critical component of all living cells. CLCs are involved in membrane potential stabilization, signal transduction, cell volume regulation and organic solute transport. The putative 247 amino acid protein chloride intracellular channel 2 (CLIC2), also designated XAP121, shares 60 % identity with the CLIC1 protein and demonstrates expression in only fetal liver and adult skeletal muscle tissues. The CLIC2 gene maps to chromosome Xq28 and contains 6 exons. Because a direct association exists between a number of human chloride channel genes and a range of hereditary diseases, CLIC2 is a potential candidate for one of the many diseases linked to Xq28. The hereditary form of incontinentia pigmenti (IP2), for example, is a rare disorder characterized by abnormalities of the tissues and organs derived from the ectoderm and neuroectoderm that has been linked to Xq28
- 途径
- Negative Regulation of Transporter Activity
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