anti-Argininosuccinate Lyase antibody

Key features and details

  • 产品描述: Rabbit Polyclonal antibody recognizes Argininosuccinate Lyase
  • 反应物种: Ms, Rat
  • 应用: WB
  • 宿主: Rabbit
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: Argininosuccinate Lyase
  • 抗原物种: Human
  • 抗原: Synthetic peptide corresponding to a sequence of Human Argininosuccinate Lyase (YTHLQRAQPIRWSHWILSHAVALTRDSERLLEVRKRIN).
  • Brand:
CAT.NO. : ARG58295
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Product Details
概述
产品描述Rabbit Polyclonal antibody recognizes Argininosuccinate Lyase
反应物种Ms, Rat
应用WB
宿主Rabbit
克隆Polyclonal
同位型IgG
靶点名称Argininosuccinate Lyase
抗原物种Human
抗原Synthetic peptide corresponding to a sequence of Human Argininosuccinate Lyase (YTHLQRAQPIRWSHWILSHAVALTRDSERLLEVRKRIN).
偶联标记Un-conjugated
別名EC 4.3.2.1; Argininosuccinate lyase; ASAL; Arginosuccinase
应用说明
应用建议
应用推荐稀释比
WB0.1 - 0.5 µg/ml
应用说明* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
属性
形式Liquid
纯化Affinity purification with immunogen.
缓冲液0.9% NaCl, 0.2% Na2HPO4, 0.05% Sodium azide and 5% BSA.
抗菌剂0.05% Sodium azide
稳定剂5% BSA
浓度0.5 mg/ml
存放说明For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项For laboratory research only, not for drug, diagnostic or other use.
生物信息
数据库连接

GeneID: 109900 Mouse ASL

GeneID: 59085 Rat ASL

Swiss-port # P20673 Rat Argininosuccinate lyase

Swiss-port # Q91YI0 Mouse Argininosuccinate lyase

基因名称ASL
全名argininosuccinate lyase
背景介绍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. [provided by RefSeq, Jul 2008]
预测分子量52 kDa
翻译后修饰Acetylation modifies enzyme activity in response to alterations of extracellular nutrient availability. Acetylation increased with trichostin A (TSA) or with nicotinamide (NAM). Glucose increases acetylation by about a factor of 3 with decreasing enzyme activity. Acetylation on Lys-288 is decreased on the addition of extra amino acids resulting in activation of enzyme activity. [UniProt]
检测图片 (1)
  • ARG58295 anti-Argininosuccinate Lyase antibody WB image

    Western blot: 50 µg of Rat liver, Rat kidney, Rat lung and Mouse liver lysates stained with ARG58295 anti-Argininosuccinate Lyase antibody at 0.5 µg/ml dilution, overnight at 4°C, under reducing conditions.

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