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ACP2 抗体 (AA 31-88) (PE)

This 兔 多克隆 antibody specifically detects ACP2 in FACS. It exhibits reactivity toward 人, 大鼠 和 小鼠.
产品编号 ABIN7965547
发货至: 中国
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Quick Overview for ACP2 抗体 (AA 31-88) (PE) (ABIN7965547)

抗原

See all ACP2 抗体
ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))

适用

  • 46
  • 31
  • 31
  • 4
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
人, 大鼠, 小鼠

宿主

  • 43
  • 3

克隆类型

  • 43
  • 3
多克隆

标记

  • 20
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ACP2 antibody is conjugated to PE

应用范围

  • 24
  • 15
  • 11
  • 8
  • 5
  • 4
  • 2
  • 1
  • 1
  • 1
Flow Cytometry (FACS)
  • 抗原表位

    • 12
    • 12
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 31-88

    原理

    Anti-ACP2 Antibody PE Conjugated

    预测反应

    Human ACP2 shares 98.3%,96.6% amino acid (aa) sequence identity with mouse,rat ACP2,respectively.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human ACP2 recombinant protein (Position: R31-H88). Human ACP2 shares 98.3% and 96.6% amino acid (aa) sequence identity with mouse and rat ACP2, respectively.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    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

    ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))

    别名

    ACP2

    背景

    Background: Lysosomal acid phosphatase is an enzyme that in humans is encoded by the ACP2 gene. The protein encoded by this gene belongs to the histidine acid phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell acid phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene in mice showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism.

    Gene Full Name: acid phosphatase 2, lysosomal

    基因ID

    53

    UniProt

    P11117
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