ABCD1 polyclonal antibody (A01)-抗體-抗體-生物在線

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亞諾法生技股份有限公司（Abnova)
ABCD1 polyclonal antibody (A01)

ABCD1 polyclonal antibody (A01)

商家詢價(jià)

產(chǎn)品名稱： ABCD1 polyclonal antibody (A01)

英文名稱： ABCD1 polyclonal antibody (A01)

產(chǎn)品編號(hào)： H00000215-A01

產(chǎn)品價(jià)格： null

產(chǎn)品產(chǎn)地： 臺(tái)灣

品牌商標(biāo)： Abnova

更新時(shí)間： null

使用范圍：

亞諾法生技股份有限公司（Abnova)
  • 聯(lián)系人 :
  • 地址 : 臺(tái)灣臺(tái)北市內(nèi)湖區(qū)洲子街 108 號(hào) 9 樓
  • 郵編 : 11493
  • 所在區(qū)域 : 臺(tái)灣
  • 電話 : +886-920**1152 點(diǎn)擊查看
  • 傳真 : 點(diǎn)擊查看
  • 郵箱 : sales@abnova.com.tw

  • Specification
  • Product Description:
  • Mouse polyclonal antibody raised against a partial recombinant ABCD1.
  • Immunogen:
  • ABCD1 (AAH15541, 1 a.a. ~ 100 a.a) partial recombinant protein with GST tag.
  • Sequence:
  • MPVLSRPRPWRGNTLKRTAVLLALAAYGAHKVYPLVRQCLAPARGLQAPAGEPTQEASGVAAAKAGMNRVFLQRLLWLLRLLFPRVLCRETGLLALHSAA
  • Host:
  • Mouse
  • Reactivity:
  • Human
  • Storage Buffer:
  • 50 % glycerol
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Quality Control Testing:
  • Antibody Reactive Against Recombinant Protein.

    QC Testing of H00000215-A01
    Western Blot detection against Immunogen (37.11 KDa) .
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Recombinant protein)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 215
  • Gene Name:
  • ABCD1
  • Gene Alias:
  • ABC42,ALD,ALDP,AMN
  • Gene Description:
  • ATP-binding cassette, sub-family D (ALD), member 1
  • Gene Summary:
  • The protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ALD subfamily, which is involved in peroxisomal import of fatty acids and/or fatty acyl-CoAs in the organelle. All known peroxisomal ABC transporters are half transporters which require a partner half transporter molecule to form a functional homodimeric or heterodimeric transporter. This peroxisomal membrane protein is likely involved in the peroxisomal transport or catabolism of very long chain fatty acids. Defects in this gene have been identified as the underlying cause of adrenoleukodystrophy, an X-chromosome recessively inherited demyelinating disorder of the nervous system. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000025960,adrenoleukodystrophy protein
  • Gene Pathway

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