TEX261 抗体 (AA 121-196)
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- 抗原 See all TEX261 products
- TEX261 (Testis Expressed 261 (TEX261))
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抗原表位
- AA 121-196
- 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 TEX261 antibody is un-conjugated
- 应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Dog,Cow,Sheep,Pig,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human TEX261
- 亚型
- IgG
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anti-Testis Expressed 261 (TEX261) (AA 148-176), (C-Term) antibody
TEX261 适用: 人 WB, FACS, IHC (p) 宿主: 兔 Polyclonal RB33130 unconjugated
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- 应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- TEX261 (Testis Expressed 261 (TEX261))
- 别名
- TEX261 (TEX261 产品)
- 别名
- TEG-261 antibody, 3110001O07Rik antibody, AA409339 antibody, AI480706 antibody, AL033351 antibody, testis expressed 261 antibody, testis expressed gene 261 antibody, TEX261 antibody, Tex261 antibody
- 背景
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Synonyms: 3110001O07Rik, AA409339, AI480706, AL033351, Protein TEX261, TEG 261, TEX261, TX261_HUMAN, UNQ1882/PRO4325.
Background: TEX261 is a 196 amino acid multi-pass membrane protein that belongs to the SVP26 family. The gene that encodes TEX261 consists of approximately 47,406 bases and maps to human chromosome 2p13.3. Consisting of 237 million bases, Chromosome 2 encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is due to mutations in the ALMS1 gene.
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