相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
- 免疫原:
A DNA sequence encoding the extracellular domain (Met 1-Arg 217) of mouse FCGR2B (NP_001070657.1) precursor was expressed 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:
50030-M08HL
- 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:
HEK293 Cells
- 应用范围:
WB
- 浓度:
见说明书
- 靶点:
FCGR2B
- 抗体英文名:
Mouse CD32 / FCGR2B HEK293 Cell Lysate (WB positive control)
- 抗体名:
Mouse CD32 / FCGR2B HEK293 Cell Lysate (WB positive control)
- 规格:
300 µg
反应种属:Mouse
裂解液靶点:FCGR2B
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:Human Cell lysate that Mouse CD32 / FCGR2B 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:HEK293 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.
风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验结果,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
糖,建议进行 Pre-clear;如果使用磁珠,此步可忽略 抗 X 抗体的轻链(25 kD)和重链(50 kD) 更侧重于如何在实验上进行优化(见下文) *注意:总蛋白上样量过多也会造成 非特异性结合,建议上样量为 500 ug-1 mg。上样之前一定要先用 BCA 定个量!定个量!定个量! pre-clear:上样前先用裂解液过一遍柱子,减少基质本身对蛋白的吸附 Output:在某些 co-IP 实验中,实验人员会把IP后的上清分别进行诱饵蛋白 X 和靶蛋白 Y 的 WB 检测
。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
技术资料暂无技术资料 索取技术资料










