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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 FCER1A (NP_001992.1) (Met1-Gln205) was expressed.
- 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:
13193-HNAHL
- 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:
0
- 浓度:
见说明书
- 靶点:
FCER1A
- 抗体英文名:
Human FCER1A / Fc epsilon RI alpha HEK293 Cell Lysate (WB positive control)
- 抗体名:
Human FCER1A / Fc epsilon RI alpha HEK293 Cell Lysate (WB positive control)
- 规格:
300 µg
反应种属:Human
裂解液靶点:FCER1A
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 Cells that Human FCER1A / Fc epsilon RI alpha Heterodimer 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.
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文献和实验Micropatterned Ligand Arrays to Study Spatial Regulation in Fc Receptor Signaling
surfaces containing spatially defined ligands are used to cluster� and activate IgE receptors (FcεRI), involved in allergic responses by mast cells. Micron-scale control of cell activation allows investigation of spatially regulated mechanisms
Capture and Qualitative Analysis of the Activated Fc Receptor Complex from Live Cells
., Saito, N., Larsson, C., Loegering, D., Weber, P.B., and Lennartz, M.R. 2002. A role for PKC‐epsilon in Fc gammaR‐mediated phagocytosis by RAW 264.7 cells. J. Cell Biol. 159:939‐944.
Introduction of human 14-3-3 proteins
regulation.We report here the crystal structure of the human T-cell 14-3-3 isoform (tau)dimer at 2.6 A resolution.Each monomer (Mr 28K)is composed of an unusual arrangement of nine antiparallel alpha-helices organized as two structural domains.The dimer
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