朊蛋白MAb QYQRES IgG1同种型

产品图片
货号/SKU
F99/97.6.1
货号/规格
0.1 mg
库存与交货期
2-4周
人民币价格

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VMRD, Inc./USA
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产品基础信息
Cell Culture Supernanent
产品描述信息
在绵羊,牛,骡鹿,麋鹿和白尾鹿的组织中,对反刍动物朊蛋白上的保守表位(QYQRES)进行了识别。 IgG1同种型。用于传染性海绵状脑病(TSEs)的检测剂,包括绵羊痒病,牛海绵状脑病(BSE),慢性消耗性疾病(CWD)。技术包括新鲜和福尔马林固定组织的免疫测定,包括Western免疫印迹(表现优于F89 / 160.1.5),免疫组织化学,ELISA和荧光流式细胞仪。通过免疫组织化学(IHC)评估来自瘙痒病的脑和淋巴结的F990803感染的绵羊,以及未知瘙痒症的绵羊的脑和淋巴结。将抗体稀释至3-5μg/ ml,并用预处理的组织孵育30分钟秒。使用生物素化的山羊抗小鼠Ig,Sterptavidin-辣根过氧化物酶和AEC作为色原/底物,在Ventana免疫染色剂上进行检测。没有暴露的绵羊组织没有受到强烈的刺激。这批抗体的质量非常好。用该抗体进行IHC的组织是石蜡包埋的福尔马林固定组织,通常通过在甲酸中将福尔马林固定的组织温育60分钟进行去污染,然后在福尔马林中重新平衡并进行常规处理和包埋。将3至5微米的部分再水化,首先用酸(98%甲酸5-20分钟,然后冲洗并用0.1M Tris缓冲液的几次更换,pH 7.5中和)进行预处理,然后加热(在121℃下高压灭菌20分钟)在改性柠檬酸盐中ffer,pH 6.1,优选DAKO Target Petrieval Buffer)。注意:该单克隆抗体作为细胞培养上清液产生,通过离心澄清,并通过0.2微米过滤器过滤。在含有4mg / ml BSA的磷酸盐缓冲盐水中,浓度为1.0mg / ml,用0.09%叠氮化钠保存。
产品安全信息
One year from date of sale
主要内容
Recongnizes a conserved epitope (QYQRES) on the ruminant prion protein in tissues from sheep, cattle, mule deer, elk and white-tailed deer. IgG1 isotype.Useful in detection agents of transmissible spongiform encephalopathies (TSEs), including sheep scrapie, bovine spongiform encephalopathy (BSE), chronic wasting disease (CWD). Techniques include immunoassays of fresh and formalin-fixed tissues, including Western immunoblot (performs better than F89/160.1.5), immunohistochemistry, ELISA, and fluorescence flow cytometry.Lot F990803 was evaluated by immunohistochemistry (IHC) of brain and lymph node from scrapie-infected sheep, and brain and lymph node from a sheep with no known exposure to scrapie. The antibody was diluted to 3-5µg/ml and incubated for 30 minutes with pretreated tissues. Detection was performed on a Ventana immunostainer using biotinylated goat anti-mouse Ig, Sterptavidin-horseradish peroxidase and AEC as the chromogen/substrate. There was no stining of the tissue from the sheep with no exposure to was intense. The quality of this lot of antibody is excellent. Tissues for IHC with this antibody are paraffin-embedded formalin-fixed tissues, often decontaminated by incubation of formalin-fixed tissue in formic Acid for 60 minutes before re-equilibration in formalin and routine processing and embedding. Three to 5 micron sections are rehydrated, pretreated first with acid (98% formic acid 5-20 minutes, then rinsed and neutralized with several changes of 0.1 M Tris buffer, pH 7.5) then with heat (autoclaved at 121°C for 20 minutes in modified citrate buffer, pH 6.1, preferably DAKO Target Petrieval Buffer). Note: This monoclonal antibody is produced as cell culture supernatant, clarified by centrifugation, and filtered though a 0.2 micron filter. The concentration is 1.0 mg/ml in phosphate-buffered saline containing 4 mg/ml BSA preserved with 0.09% sodium azide.
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