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NIPAL2 抗体 (AA 1-100) (FITC)

This anti-NIPAL2 antibody is a 兔 多克隆 antibody detecting NIPAL2 in WB, IF (cc) 和 IF (p). Suitable for 小鼠.
产品编号 ABIN1389248
发货至: 中国

Quick Overview for NIPAL2 抗体 (AA 1-100) (FITC) (ABIN1389248)

抗原

NIPAL2 (NIPA-Like Domain Containing 2 (NIPAL2))

适用

  • 22
  • 12
  • 1
  • 1
小鼠

宿主

  • 26

克隆类型

  • 26
多克隆

标记

  • 8
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NIPAL2 antibody is conjugated to FITC

应用范围

  • 26
  • 12
  • 12
  • 11
  • 3
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 8
    • 4
    • 1
    AA 1-100

    交叉反应

    小鼠

    预测反应

    Human,Rat,Cow,Sheep,Pig,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human NIPAL2

    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

    NIPAL2 (NIPA-Like Domain Containing 2 (NIPAL2))

    别名

    NIPAL2

    背景

    Synonyms: NIPA like domain containing 2, NIPAL2, NPAL2, NPAL2_HUMAN.

    Background: Non-imprinted in Prader-Willi/Angelman syndrome (NIPA) proteins are highly conserved receptors or transporters. A family known as the NIPA-like domain containing (NPAL) proteins are closely related to the NIPA proteins, but most are uncharacterized and their functions are unknown. NPAL2 (NIPA-like domain containing 2), also known as NIPAL2, is a 368 amino acid multi-pass membrane protein belonging to the NIPA family and is encoded by a gene located on human chromosome 8. Human chromosome 8 consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.

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