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ADA 抗体 (AA 80-160)

This 兔 多克隆 anti-ADA antibody specifically detects ADA in WB 和 ELISA. The antibody is reactive with 人 samples.
产品编号 ABIN7227210
发货至: 中国
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Quick Overview for ADA 抗体 (AA 80-160) (ABIN7227210)

抗原

See all ADA 抗体
ADA (Adenosine Deaminase (ADA))

适用

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宿主

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克隆类型

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多克隆

标记

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This ADA antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA
  • 抗原表位

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    AA 80-160

    原理

    ADA Polyclonal Antibody

    特异性

    The antibody detects endogenous levels of ADA protein

    纯化方法

    The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen

    免疫原

    Synthesized peptide derived from part region of human ADA protein at AA range: 80-160

    亚型

    IgG
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).

    说明

    Primary Antibody

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

    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

    Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
  • 抗原

    ADA (Adenosine Deaminase (ADA))

    别名

    ADA

    背景

    Rabbit Anti-ADA Polyclonal Antibody,Adenosine deaminase, Adenosine aminohydrolase,ADA (Adenosine Deaminase) is a Protein Coding gene. Diseases associated with ADA include Severe Combined Immunodeficiency Due To Ada Deficiency and Adenosine Deaminase Deficiency. Among its related pathways are Metabolism and One carbon pool by folate. ADA encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for ADA and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia.,ADA

    基因ID

    100

    UniProt

    P00813

    途径

    Regulation of G-Protein Coupled Receptor Protein Signaling, Ribonucleoside Biosynthetic Process
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