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TEX261 抗体 (AA 121-196)

This anti-TEX261 antibody is a 兔 多克隆 antibody detecting TEX261 in ELISA, IHC (p), ICC, IF (cc), IF (p) 和 IHC (fro). Suitable for 人.
产品编号 ABIN1386683
发货至: 中国

Quick Overview for TEX261 抗体 (AA 121-196) (ABIN1386683)

抗原

TEX261 (Testis Expressed 261 (TEX261))

适用

宿主

  • 9

克隆类型

  • 9
多克隆

标记

  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
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))
  • 抗原表位

    • 8
    • 2
    • 1
    AA 121-196

    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
  • 应用备注

    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
  • 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
  • 抗原

    TEX261 (Testis Expressed 261 (TEX261))

    别名

    TEX261

    背景

    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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