ELISA试剂盒我们提供的抗体用于实验研究，而不用于诊临床断或治疗程序。
细胞酪氨酸转氨酶抗体Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
英文名称 Anti-ATTY 
中文名称 细胞酪氨酸转氨酶抗体 
别 名 TYROSINE AMINOTRANSFERASE; tyrosine aminotransferase; MGC37772; MGC37789; MGC37790; MGC37819; MGC37828; MGC37842; TAT; ATTY_HUMAN; L-tyrosine:2-oxoglutarate aminotransferase; TAT; Tyrosine aminotransferase; Tyrosine aminotransferase, cytosolic. 
浓 度 1mg/1ml 
规 格 0.2ml/200μg 
细胞酪氨酸转氨酶抗体抗体来源 Rabbit 
克隆类型 polyclonal 
交叉反应 Human, Mouse, Rat, Cow 
产品类型 一抗 
研究领域 细胞生物 神经生物学 信号转导 激酶和磷酸酶 合成与降解 
蛋白分子量 predicted molecular weight: 50kDa 
性 状 Lyophilized or Liquid 
免 疫 原 KLH conjugated synthetic peptide derived from human Tat 
亚 型 IgG 
纯化方法 affinity purified by Protein A 
储 存 液 0.01M PBS, pH 7.4 with 10 mg/ml BSA and 0.1% Sodium azide 
产品应用 WB=1:100-500 ELISA=1:500-1000 IP=1:20-100 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 
（石蜡切片需做抗原修复） 
not yet tested in other applications. 
optimal dilutions/concentrations should be determined by the end user. 
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. 
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 
产品介绍 This nuclear gene encodes a mitochondrial protein tyrosine aminotransferase which is present in the liver and catalyzes the conversion of L-tyrosine into p-hydroxyphenylpyruvate. Mutations in this gene cause tyrosinemia （type II, Richner-Hanhart syndrome）, a disorder accompanied by major skin and corneal lesions, with possible mental retardation. A regulator gene for tyrosine aminotransferase is X-linked. 
Function : Transaminase involved in tyrosine breakdown. Converts tyrosine to p-hydroxyphenylpyruvate. Can catalyze the reverse reaction, using glutamic acid, with 2-oxoglutarate as cosubstrate （in vitro）. Has no transaminase activity towards phenylalanine. 
Subunit : Homodimer （Probable）. 
ELISA试剂盒DISEASE : Defects in TAT are the cause of tyrosinemia type 2 （TYRO2） [MIM:276600]; also known as Richner-Hanhart syndrome. TYRO2 is an inborn error of metabolism characterized by elevations of tyrosine in the blood and urine, and oculocutaneous manifestations. Typical features include palmoplantar keratosis, painful corneal ulcers, and mental retardation. 
Similarity : Belongs to the class-I pyridoxal-phosphate-dependent aminotransferase family.