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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 IL17C (NP_037410.1) (Met1-Val197) 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:
Human
- 保质期:
12个月
- 抗原来源:
见说明书
- 目录编号:
10784-H02BL
- 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:
0
- 浓度:
见说明书
- 靶点:
IL17C
- 抗体英文名:
Human IL-17C / IL17C Insect Cells Cell Lysate (WB positive control)
- 抗体名:
Human IL-17C / IL17C Insect Cells Cell Lysate (WB positive control)
- 规格:
300 µg
反应种属:Human
裂解液靶点:IL17C
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 Cells that Human IL-17C / IL17C 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: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Human IL-2 Enzyme Immunoassay (EIA)
2 EIA is an in vitro enzyme-linked immunosorbent assay for quantitatively detecting human IL-2 in biological fluids (e.g. serum, plasma) and in cell culture supernatants. The kit consists of a 96 well microtiter plate that has been precoated with anti-IL-
, cryopreserving, and thawing human PBMCs; and finally, detecting vaccinia-specific IL-10 and IFNγ secreting lymphocytes, as well as CD8+ IFNγ T cells following in vitro stimulation of PBMCs with vaccinia virus. The methods presented below, although optimized
Potentiated autologous tumor cell and peripheral blood lymphocyte lysate vaccination
its own antibodies. Autologous tumor-cell vaccination has no contraindications or side-effects, since the patients own materials (lymphocytes, tumor cells) are used. We describe a method for producing an autologous cancer vaccine. The material to be injected
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