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Adracalin Protein (DYKDDDDK Tag)

AAAS 宿主: 人 宿主: Insect cells (Sf9) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2714524
发货至: 中国
  • 抗原 See all Adracalin (AAAS) 蛋白
    Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
    蛋白类型
    Recombinant
    宿主
    • 3
    • 1
    资源
    • 2
    • 2
    Insect cells (Sf9)
    标记
    This Adracalin protein is labelled with DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Aladin (full length, C-term DDK tag, transcript variant 1) protein expressed in Sf9 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product AAAS 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    50 mM Tris-HCl, pH 8.0, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    Adracalin (AAAS) (Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS))
    别名
    Aladin (AAAS 产品)
    别名
    zgc:85873 Protein, aladin Protein, Aladin Protein, AAA Protein, AAASb Protein, ADRACALA Protein, ADRACALIN Protein, ALADIN Protein, D030041N15Rik Protein, GL003 Protein, aladin WD repeat nucleoporin Protein, achalasia, adrenocortical insufficiency, alacrimia Protein, aladin WD repeat nucleoporin L homeolog Protein, Aaas Protein, aaas Protein, aaas.L Protein, AAAS Protein
    背景
    The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene.
    分子量
    59.4 kDa
    NCBI登录号
    NP_056480
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