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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 rhesus ICOS (NP_001253918.1) (Met1-Lys140) was expressed with the Fc region of human IgG1 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:
Rhesus
- 保质期:
12个月
- 抗原来源:
见说明书
- 目录编号:
90866-C02HL
- 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:
ICOS
- 抗体英文名:
Rhesus ICOS / AILIM / CD278 CHO Cell Lysate (WB positive control)
- 抗体名:
Rhesus ICOS / AILIM / CD278 CHO Cell Lysate (WB positive control)
- 规格:
300 µg
反应种属:Rhesus
裂解液靶点:ICOS
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:HEK293 Cell Rhesus ICOS / AILIM / CD278 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 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. 3. Store the lyophilized cell lysate at 4℃. After re-dissolution, recommend to aliquot it into smaller quantities and store at -80℃.
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.
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文献和实验264.7 细胞进行 EST12-His pull-down 实验,WB 分析;B:共聚焦显微镜分析分别转染 pEGFP-C1-EST12 和 pAsRED2-C1-RACK1 的 RAW264.7 细胞;C:WB 和 qPCR 分析 2μM EST12 刺激的 RAW264.7 细胞;D、E:LDH、ELISA 分析 2μM EST12 处理 WT 和 RACK1−/−腹腔巨噬细胞上清;F:WB 检测细胞裂解液中 GSDMD 和 caspase-1;G:2μM EST12 处理和 PI 染色 WT、RACK
效率(尤其是使用后期)的关系并不稳定,单纯依靠时间有时会有问题。 蛋白来源:CHO cell 蛋白名称(可保密):酶原 蛋白分子量:40 KD WB用膜类型、孔径:0.22的PVDF膜(Biorad
便于纯化 有时会出现蛋白切割问题 糖基化不能满足要求 昆虫 High-5 产量高 ,翻译后加工与哺乳动物相似 对于部分有毒性或较难表达蛋白有优势 无内毒素污染 蛋白活性不如哺乳动物 适合表达激酶等定位于细胞内的真核蛋白 哺乳 CHO HEK293 完善的翻译后加工,活性接近
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