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- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
A DNA sequence encoding the mouse AARS (Q8BGQ7) (Met 1-Asn 968) was fused with a polyhistidine tag at the C-terminus.
- 亚型:
见说明书
- 形态:
液体
- 保存条件:
4℃
- 克隆性:
无
- 标记物:
见说明书
- 适应物种:
Mouse
- 保质期:
12个月
- 抗原来源:
见说明书
- 目录编号:
50384-M08BL
- 级别:
免疫学
- 库存:
99
- 供应商:
北京义翘神州科技股份有限公司
- 宿主:
Baculovirus-Insect cells
- 应用范围:
WB
- 浓度:
见说明书
- 靶点:
AARS
- 抗体英文名:
Mouse AARS / alanyl-tRNA synthetase Insect Cell Lysate (WB positive control)
- 抗体名:
Mouse AARS / alanyl-tRNA synthetase Insect Cell Lysate (WB positive control)
- 规格:
300 µg
反应种属:Mouse
裂解液靶点:AARS
裂解液应用:WB
裂解液保存条件:Store at 4℃. After re-dissolution, aliquot and store at -80℃.
裂解液产品描述:Baculovirus-Insect Cell lysate that Mouse AARS / alanyl-tRNA synthetase transfected / overexpressed for Western blot (WB) positive control. The whole cell lysate is provided in 1X Sample Buffer (1X modified RIPA buffer+1X SDS loading buffer).
裂解液表达宿主:Baculovirus-Insect cells
裂解液制备方法:Cell lysate was prepared by homogenization of the over-expressed cells in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined by Bradford assay (Bio-Rad protein assay, Microplate Standard assay). The cell lysate was boiled for 5 min in 1 x SDS loading buffer (50 mM Tris-HCl pH 6.8, 12.5% glycerol, 1% sodium dodecylsulfate, 0.01% bromophenol blue) containing 5% b-mercaptoethanol, and lyophilized.
裂解液Buffer:Modified RIPA Lysis Buffer: 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.
裂解液质控信息:12.5% SDS-PAGE Stained with Coomassie Blue after protein purification.
裂解液使用建议:1. Centrifuge the tube for a few seconds and ensure the pellet at the bottom of the tube. 2. Re-dissolve the pellet using 200μL pure water and boil for 2-5 min.
裂解液稳定性:Samples are stable for up to twelve months from date of receipt.
裂解液使用说明:Western blot (WB): Use at an assay dependent dilution. Other Applications: Not tested. Optimal dilutions/concentrations should be determined by the end user.
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文献和实验628895 CD44 抗体是小鼠单克隆抗体,使用基因敲除的细胞裂解液进行验证,可看到处理后条带消失,证实抗体特异性辨识 CD44 蛋白。GTX628895 还适用多种应用,包括 WB、IHC-P、FACS 和 IP,及多篇文献引用,为可靠的抗体工具。2. 比较抗体验证天下风云豪杰出,一入江湖天下知,刀剑交锋断柔情,青史惟有王者留。好抗体比了才知道,相同靶标、相同处理的样品,理论上抗体辨识的条带位置应该相同。如不相同,可能有其一抗体辨识错误蛋白或是其他原因;另外也可以通过比较找到更高敏的抗体。以乳癌标记
结果,将NC膜晾干扫描保存。反应溶液可预先配置,可在4℃储存一年以上。 三、说明 1. WB对照系统 阳性对照:最好有标准品,或阳性血清、阳性上清。 阴性对照:测血时用相应小鼠未免疫血清,测培养上清,用无克隆培养上清。 空白对照:不加一抗,用1%BSA代替。 无关对照(替代对照):用无关项目一抗,或无关项目的抗体。 2.切割膜时,大小一般为3-5mm,一抗的体积为每条膜保证1ml。 3.KSHV、MCMV
。下面是来自使用者的反馈数据: 1、蛋白含量低,得到的WB信号弱--SignalBoostTM可以增强信号,检测到低丰度蛋白: 样品:K562细胞全细胞裂解液。 (Lane 1: 25μg总蛋白;Lane 2: 5μg总蛋白;Lane 3: 2.5μg总蛋白) 一抗:anti-PKC(Ab-2)小鼠单抗(MC5)(货号OP74),分别用5%脱脂奶粉PBST溶液(图A)和SignalBoost Solution 1(图B)按照1:1000比例稀释。 二抗:Rabbit anti
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