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ASL 抗体

This anti-ASL antibody is a 兔 多克隆 antibody detecting ASL in WB 和 ELISA. Suitable for 人, 小鼠, 大鼠 和 犬.
产品编号 ABIN2462448
发货至: 中国

Quick Overview for ASL 抗体 (ABIN2462448)

抗原

See all ASL 抗体
ASL (Argininosuccinate Lyase (ASL))

适用

  • 60
  • 14
  • 10
  • 6
  • 6
  • 6
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  • 4
  • 4
  • 3
  • 3
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  • 2
人, 小鼠, 大鼠, 犬

宿主

  • 55
  • 5

克隆类型

  • 57
  • 3
多克隆

标记

  • 31
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ASL antibody is un-conjugated

应用范围

  • 40
  • 13
  • 13
  • 13
  • 12
  • 12
  • 7
  • 6
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by protein A chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ASL.
  • 应用备注

    ASL antibody can be used for detection of ASL by ELISA at 1:62500. ASL antibody can be used for detection of ASL by western blot at 5.0 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store ASL antibody at -20 °C.
  • 抗原

    ASL (Argininosuccinate Lyase (ASL))

    别名

    ASL

    背景

    ASL is a member of the lyase 1 family. The protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in its gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency.This gene encodes a member of the lyase 1 family. The encoded protein forms a cytosolic homotetramer and primarily catalyzes the reversible hydrolytic cleavage of argininosuccinate into arginine and fumarate, an essential step in the liver in detoxifying ammonia via the urea cycle. Mutations in this gene result in the autosomal recessive disorder argininosuccinic aciduria, or argininosuccinic acid lyase deficiency. A nontranscribed pseudogene is also located on the long arm of chromosome 22. Alternatively spliced transcript variants encoding different isoforms have been described.

    分子量

    49 kDa, 52 kDa, 52 kDa, 49 kDa

    基因ID

    435

    NCBI登录号

    NP_001020115

    UniProt

    P04424

    途径

    Response to Growth Hormone Stimulus
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