Sorting Nexin 7 抗体 (AA 151-250) (Biotin)
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- 抗原 See all Sorting Nexin 7 (SNX7) 抗体
- Sorting Nexin 7 (SNX7)
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抗原表位
- AA 151-250
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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 Sorting Nexin 7 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SNX7
- 亚型
- IgG
- Top Product
- Discover our top product SNX7 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
- Sorting Nexin 7 (SNX7)
- 别名
- SNX7 (SNX7 产品)
- 别名
- zgc:92458 antibody, SNX7 antibody, 2510028H01Rik antibody, sorting nexin 7 antibody, sorting nexin-7 antibody, SNX7 antibody, snx7 antibody, LOC715581 antibody, LOC716015 antibody, Snx7 antibody
- 背景
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Synonyms: MGC8717, DKFZP564F052, MGC8717, MGC8717, , Sorting nexin 7, Sorting nexin 7 isoform a, SNX7_HUMAN.
Background: Sorting nexin (SNX) proteins are members of a large family of hydrophilic PX (phospholipid-binding motif) domain-containing proteins that interact with a variety of receptor types. SNXs are widely expressed, although the tissue distribution of each SNX mRNA varies. The ability of SNXs to bind specific phospholipids, as well as their tendency to form protein-protein complexes, suggests a role for these proteins in cellular membrane trafficking and protein sorting. SNXs may also function specifically in pro-degradative sorting, internalization, endosomal recycling or simply in endosomal sorting. SNXs partially associate with cellular membranes, despite their hydrophilic nature. SNX7 is unique in that it does not have a coiled coil region like some of the SNX family members. Mutations in the SNX7 gene have not been shown to cause any diseases.
- 基因ID
- 51375
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