电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

AMPD1 抗体 (AA 50-260)

This anti-AMPD1 antibody is a 兔 多克隆 antibody detecting AMPD1 in WB 和 IF. Suitable for 人.
产品编号 ABIN1678653
发货至: 中国

Quick Overview for AMPD1 抗体 (AA 50-260) (ABIN1678653)

抗原

See all AMPD1 抗体
AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

适用

  • 30
  • 23
  • 23
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2

宿主

  • 37
  • 1

克隆类型

  • 38
多克隆

标记

  • 14
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This AMPD1 antibody is un-conjugated

应用范围

  • 14
  • 13
  • 13
  • 10
  • 6
  • 3
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (IF)
  • 抗原表位

    • 15
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 50-260

    序列

    AEKVFASEVK DEGGRQEISP FDVDEICPIS HHEMQAHIFH LETLSTSTEA RRKKRFQGRK TVNLSIPLSE TSSTKLSHID EYISSSPTYQ TVPDFQRVQI TGDYASGVTV EDFEIVCKGL YRALCIREKY MQKSFQRFPK TPSKYLRNID GEAWVANESF YPVFTPPVKK GEDPFRTDNL PENLGYHLKM KDGVVYVYPN EAAVSKDEPK P

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 50-260 of human AMPD1 (NP_001166097.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    限制

    仅限研究用
  • 缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

    别名

    AMPD1

    背景

    Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.,AMPD1,MAD,MADA,MMDD,Cancer,Signal Transduction,Endocrine & Metabolism,AMPD1

    分子量

    89 kDa/90 kDa

    基因ID

    270

    UniProt

    P23109
You are here:
Chat with us!