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Anti-Adenylosuccinate Lyase/FITC抗体
产品编号YB-6352R-FITC
英文名称Anti-Adenylosuccinate Lyase/FITC
中文名称FITC标记的腺苷酸琥珀酸裂解酶抗体
别 名Adenylosuccinase; Adenylosuccinate lyase; ADSL; AMPS; ASase; ASL; PUR8_HUMAN.
Anti-Adenylosuccinate Lyase/FITC抗体
说 明 书100ul
研究领域细胞生物 信号转导
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat, Dog, Pig, Cow, Horse,
产品应用IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量55kDa
性 状Lyophilized or Liquid
浓 度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human Adenylosuccinate Lyase
亚 型IgG
纯化方法affinity purified by Protein A
储 存 液Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4
保存条件Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Anti-Adenylosuccinate Lyase/FITC抗体
产品介绍background:
Adenylsuccinate lyase is involved in both de novo synthesis of purines and formation of adenosine monophosphate from inosine monophosphate. It catalyzes two reactions in AMP biosynthesis: the removal of a fumarate from succinylaminoimidazole carboxamide (SAICA) ribotide to give aminoimidazole carboxamide ribotide (AICA) and removal of fumarate from adenylosuccinate to give AMP. Adenylosuccinase deficiency results in succinylpurinemic autism, psychomotor retardation, and , in some cases, growth retardation associated with muscle wasting and epilepsy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Tissue Specificity:
Ubiquitously expressed. Both isoforms are produced by all tissues. Isoform 2 is 10-fold less abundant than isoform 1.
DISEASE:
Defects in ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency) . Anti-Adenylosuccinate Lyase/FITC抗体ADSL deficiency is an autosomal recessive disorder characterized by the accumulation in the body fluids of succinylaminoimidazole-carboxamide riboside (SAICA-riboside) and succinyladenosine (S-Ado). Most children display marked psychomotor delay, often accompanied by epilepsy or autistic features, or both, although some patients may be less profoundly retarded. Occasionally, growth retardation and muscular wasting are also present.
Similarity:
Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily.
Anti-Adenylosuccinate Lyase/FITC抗体Database links:
Entrez Gene: 158 Human
Entrez Gene: 11564 Mouse
Entrez Gene: 315150 Rat
Omim: 608222 Human
SwissProt: P30566 Human
SwissProt: P54822 Mouse
Unigene: 75527 Human
Unigene: 38151 Mouse
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.