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OPLAH 抗体 (AA 788-1072)

This anti-OPLAH antibody is a 兔 多克隆 antibody detecting OPLAH in WB, ELISA, FACS, ICC 和 IF. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN7602454
发货至: 中国
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Quick Overview for OPLAH 抗体 (AA 788-1072) (ABIN7602454)

抗原

See all OPLAH 抗体
OPLAH (5-Oxoprolinase (ATP-Hydrolysing) (OPLAH))

适用

人, 小鼠, 大鼠

宿主

  • 7

克隆类型

  • 7
多克隆

标记

  • 7
This OPLAH antibody is un-conjugated

应用范围

Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • 抗原表位

    • 2
    • 2
    • 1
    • 1
    AA 788-1072

    原理

    Anti-OPLAH Antibody

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    产品特性

    Anti-OPLAH Antibody (ABIN7602454). Tested in ELISA, Flow Cytometry, IF, ICC, WB applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human OPLAH recombinant protein (Position: H788-E1072).

    亚型

    IgG
  • 应用备注

    Western blot, 0.25-0.5 μg/mL, Human, Mouse, Rat
    Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
    Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
    ELISA, 0.1-0.5 μg/mL, -

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    浓度

    500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
  • 抗原

    OPLAH (5-Oxoprolinase (ATP-Hydrolysing) (OPLAH))

    别名

    OPLAH

    背景

    Synonyms: Protein eva-1 homolog A, Protein FAM176A, Transmembrane protein 166, EVA1A, FAM176A, TMEM166, SP24

    Tissue Specificity: Expressed in lung, kidney, liver, pancreas, placenta, but not in heart and skeletal muscle.

    Background: The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD).

    分子量

    140 kDa

    基因ID

    26873

    UniProt

    O14841
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