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NIPAL3 抗体 (AA 1-100) (Cy5)

This anti-NIPAL3 antibody (ABIN1407142) is a Rabbit Polyclonal antibody detecting NIPAL3 in WB, IF (cc), IF (p). Suitable for Human.
产品编号 ABIN1407142
发货至: 中国

Quick Overview for NIPAL3 抗体 (AA 1-100) (Cy5) (ABIN1407142)

抗原

NIPAL3 (NIPA-Like Domain Containing 3 (NIPAL3))

适用

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宿主

  • 25
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克隆类型

  • 26
多克隆

标记

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This NIPAL3 antibody is conjugated to Cy5

应用范围

  • 26
  • 12
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  • 10
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  • 5
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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 8
    • 3
    • 1
    • 1
    AA 1-100

    交叉反应

    预测反应

    Mouse,Rat,Cow,Sheep,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human NIPAL3

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    NIPAL3 (NIPA-Like Domain Containing 3 (NIPAL3))

    别名

    NIPAL3

    背景

    Synonyms: NPAL3, NPAL-3, NIPA like domain containing 3, NIPA like protein 3, RGD1563439, RP23-332E2.5, RP3-462O23.3, NPAL3_HUMAN.

    Background: NIPAL3 is a 406 amino acid multi-pass membrane protein that belongs to the NIPA family and exists as three alternatively spliced isoforms. The gene that encodes NPAL3 consists of approximately 57,229 bases and maps to human chromosome 1p36. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

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