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LRRC2 抗体 (AA 1-100) (Biotin)

This anti-LRRC2 antibody is a 兔 多克隆 antibody detecting LRRC2 in WB, ELISA, IHC (fro) 和 IHC (p). Suitable for 小鼠 和 大鼠.
产品编号 ABIN1398631
发货至: 中国
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中国
北京 101111
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Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for LRRC2 抗体 (AA 1-100) (Biotin) (ABIN1398631)

抗原

See all LRRC2 抗体
LRRC2 (Leucine Rich Repeat Containing 2 (LRRC2))

适用

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小鼠, 大鼠

宿主

  • 28
  • 5

克隆类型

  • 31
  • 2
多克隆

标记

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This LRRC2 antibody is conjugated to Biotin

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 14
    • 7
    • 3
    • 3
    • 2
    • 2
    • 1
    AA 1-100

    交叉反应

    小鼠, 大鼠

    预测反应

    Human,Dog,Cow,Sheep,Pig,Horse

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human LRRC2

    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.

    储存条件

    -20 °C

    储存方法

    Store at -20°C for 12 months.

    有效期

    12 months
  • 抗原

    LRRC2 (Leucine Rich Repeat Containing 2 (LRRC2))

    别名

    LRRC2

    背景

    Synonyms: Leucine rich repeat containing 2, LRRC2_HUMAN.

    Background: The leucine-rich repeat-containing protein 2 (LRRC2) is a 371 amino acid protein that contains 9 LRR repeats. The gene encoding LRRC2 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

    基因ID

    79442
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