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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 human WWP2 (O00308) (Met1-Glu870) was fused with the N-terminal polyhistidine-tagged GST tag at the N-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:
Human
- 保质期:
12个月
- 抗原来源:
见说明书
- 目录编号:
13125-H20BL
- 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:
WWP2
- 抗体英文名:
Human WWP2 Insect Cell Lysate (WB positive control)
- 抗体名:
Human WWP2 Insect Cell Lysate (WB positive control)
- 规格:
300 µg
反应种属:Human
裂解液靶点:WWP2
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 Human WWP2 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of paraoxonase-1 activity in lysate The bioactivity of paraoxonase-1 present in the cell lysate was demonstrated by its ability to hydrolyse 4 mM phenyl acetate in 20 mM Tris HCl buffer pH 8.0, containing 1 mM CaCl2. As a control 10 mM EDTA was added
Retroviral Gene Expression Control in Primary Organoid Cultures
and biological inhibitors or activators. This method provides a novel, versatile tool for phenotypic analysis of endodermal epithelium in vitro. Curr. Protoc. Stem Cell Biol . 27:5A.6.1?5A.6.8. © 2013 by John Wiley & Sons, Inc. Keywords
total RNA came from independent cell cultures. Data are shown as relative cycling times (ΔCT) calculated with endogenous control RNU18 for ME-15 (color-filled bars ) and HuH7 (gray ). Error bars represent ΔCT ± Δx (standard deviation of biological
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