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TEX43 抗体 (AA 51-134) (HRP)

TEX43 适用: 人 ELISA, WB, IHC (fro), IHC (p) 宿主: 兔 Polyclonal HRP
产品编号 ABIN1712020
发货至: 中国
  • 抗原 See all TEX43 products
    TEX43 (Testis expressed 43 (TEX43))
    抗原表位
    • 14
    • 6
    AA 51-134
    适用
    宿主
    • 19
    • 1
    克隆类型
    • 19
    • 1
    多克隆
    标记
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TEX43 antibody is conjugated to HRP
    应用范围
    • 15
    • 13
    • 13
    • 7
    • 2
    • 2
    • 1
    • 1
    ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    预测反应
    Human,Mouse,Rat,Dog,Cow,Horse,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C5orf48
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    限制
    仅限研究用
  • 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.
    注意事项
    Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    TEX43 (Testis expressed 43 (TEX43))
    别名
    C5orf48 (TEX43 产品)
    别名
    Tseg7 antibody, testis expressed 43 antibody, TEX43 antibody, Tex43 antibody
    背景

    Synonyms: C5orf48, CE048_HUMAN, Chromosome 5 open reading frame 48, Uncharacterized protein C5orf48.

    Background: C5orf48 (chromosome 5 open reading frame 48), also known as FLJ27505, MGC163367 or MGC163369, is a 134 amino acid protein. Encoded by a gene that maps to human chromosome 5q23.2, C5orf48 is linked to Autosomal dominant leukodystrophy (ADLD). Chromosome 5 makes up approximately 6 % of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

    基因ID
    389320
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