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SMIM14 抗体 (AA 1-50)

This 兔 多克隆 anti-SMIM14 antibody specifically detects SMIM14 in ELISA, ICC, IF (cc), IF (p), IHC (fro) 和 IHC (p). The antibody is reactive with 人 samples.
产品编号 ABIN1714043
发货至: 中国
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Quick Overview for SMIM14 抗体 (AA 1-50) (ABIN1714043)

抗原

SMIM14 (Small Integral Membrane Protein 14 (SMIM14))

适用

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宿主

  • 15

克隆类型

  • 15
多克隆

标记

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This SMIM14 antibody is un-conjugated

应用范围

ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

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    AA 1-50

    预测反应

    Human,Mouse,Rat,Dog,Cow,Chicken

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human C4orf34

    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

    SMIM14 (Small Integral Membrane Protein 14 (SMIM14))

    别名

    C4orf34

    背景

    Synonyms: Chromosome 4 open reading frame 34, Uncharacterized protein C4orf34, SIM14_HUMAN.

    Background: C4orf34 (chromosome 4 open reading frame 34) is a 99 amino acid single-pass membrane protein that is encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

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