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发布时间:2024-02-06 浏览量:300
订购热线:0551-66199177
说明书:说明书
价格:1138元
产品编号 bs-10958R
基因名称 SLC32A1
别名 VGAT: bA12201.1: GABA and glycine transporter; hVIAAT: SLC32A 1: solute carier family 32 (GABA vesicular transporter) member 1: Solute carrier family 32 member 1: Vesicular GABA Amino Acid Transporter, Vesicular GABA transporter, Vesicular inhibitory amino acid transporter. VGAT: VIAAT: VIAAT HUMAN
抗体宿主 abbit
克隆 Polyclonal
种属反应性 dicted: Human, Mouse, Rat, Pig, Cow, Rabbit, Sheep, )
产品应用

IHC-P=1:100-500 1HC-F=1:100-500CC=1:100-500 F=1:100-500 (石切片需做抗原修复)

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

分子量 57kDa
UniProt ID
NCBI Gene
性状 Liquid
浓度 1mg/ml
同种型 IgG
纯化方法 affinity purified by Protein A
缓冲液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Procin300 and 50% Glycerol
保存条件 Shipped at 4°C. Store at -20 “C for one year. Avoid repeated freeze/thaw cycles
注意事项 This product as supplied is intended for research use only not for use in human, therapeutic or diagnostic applications
产品背景 Biotin, also known as vitamin B7, is an essential water-soluble vitamin that is a cofactor in glucogenesis and in the metabolism of fatty acids and leucine. Biotinidase is a 523 amino acid enzyme that catalyzes the hydrolysis of biocytin to biotin and lysine. Secreted into extracellular space, biotinidase is expressed in liver, heart, placenta, brain, skeletal muscle, pancreas and kidney. Biotinidase contains one carbon-nitrogen hydrolase domain, which is involved in the reduction of organic nitrogen compounds and ammonia production. Defects in the gene encoding biotinidase are the cause of biotinidase deficiency, which is characterized by skin rash, ataxia, seizures, hearing loss, hypotonia and optic atrophy. These symptoms are due to the individual’s inability to reutilize biotin and can, therefore, typically be treated with the addition of free biotin.
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