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PNPT1 抗体 (AA 1-257) (Cy3)

This 兔 多克隆 antibody specifically detects PNPT1 in FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN8024453
发货至: 中国
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Quick Overview for PNPT1 抗体 (AA 1-257) (Cy3) (ABIN8024453)

抗原

See all PNPT1 抗体
PNPT1 (Polyribonucleotide Nucleotidyltransferase 1 (PNPT1))

适用

  • 49
  • 35
  • 31
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
人, 小鼠, 大鼠

宿主

  • 63
  • 3

克隆类型

  • 65
  • 1
多克隆

标记

  • 30
  • 5
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PNPT1 antibody is conjugated to Cy3

应用范围

  • 50
  • 22
  • 16
  • 13
  • 13
  • 12
  • 10
  • 9
  • 9
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
Flow Cytometry (FACS)
  • 抗原表位

    • 15
    • 12
    • 7
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-257

    原理

    Anti-PNPT1 Antibody Cy3 Conjugated

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human PNPT1 recombinant protein (Position: M1-Q257).

    亚型

    IgG
  • 应用备注

    Flow Cytometry, 1-3 μg/1x106 cells

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    PNPT1 (Polyribonucleotide Nucleotidyltransferase 1 (PNPT1))

    别名

    PNPT1

    背景

    Background: The protein encoded by this gene belongs to the evolutionary conserved polynucleotide phosphorylase family comprised of phosphate dependent 3'-to-5' exoribonucleases implicated in RNA processing and degradation. This enzyme is predominantly localized in the mitochondrial intermembrane space and is involved in import of RNA to mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency-13 and autosomal recessive nonsyndromic deafness-70. Related pseudogenes are found on chromosomes 3 and 7.

    Gene Full Name: polyribonucleotide nucleotidyltransferase 1

    基因ID

    87178

    UniProt

    Q8TCS8
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