Sorting Nexin 7 抗体 (AA 151-250) (Cy5)
Quick Overview for Sorting Nexin 7 抗体 (AA 151-250) (Cy5) (ABIN1704995)
抗原
See all Sorting Nexin 7 (SNX7) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 151-250
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预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human SNX7
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亚型
- IgG
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anti-Sorting Nexin 7 (SNX7) (AA 85-330) antibody
SNX7 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Sorting Nexin 7 (SNX7) (AA 1-336) antibodySNX7 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Sorting Nexin 7 (SNX7) (AA 359-408) antibodySNX7 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Sorting Nexin 7 (SNX7) (AA 85-330) antibodySNX7 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- Sorting Nexin 7 (SNX7)
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别名
- SNX7
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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.
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基因ID
- 51375
抗原
-
