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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 NKG2D (NP_031386.2) (Phe78-Val216) was expressed with the Fc region of human IgG1 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:
10575-H01SL
- 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:
CHO Stable Cells
- 应用范围:
WB
- 浓度:
见说明书
- 靶点:
KLRK1
- 抗体英文名:
Human NKG2D / CD314 / KLRK1 CHO Cell Lysate (WB positive control)
- 抗体名:
Human NKG2D / CD314 / KLRK1 CHO Cell Lysate (WB positive control)
- 规格:
300 µg
反应种属:Human
裂解液靶点:KLRK1
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:CHO lysate that Human NKG2D / CD314 / KLRK1 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:CHO Stable 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Immunoblotting. Sci Signal. ; 8(371): rs2. doi:10.1126/scisignal.2005966.➤ 研究方法1. MCF10A-5E 人乳腺上皮细胞激活 Fas 死亡受体,无激活组为对照2. 分别用 NP-40(不含 SDS 和脱氧胆酸盐),RIPA buffer, Laemmil(SB)样品缓冲液提取蛋白3. WB 进行 Clv-caspase-8 检测, Hsp90,Tubulin,P38 作为对照➤ 主要发现结果显示,仅在 Laemmil 缓冲液提取的样品中检测
. Sci Signal. ; 8(371): rs2. doi:10.1126/scisignal.2005966.■ 研究方法1. MCF10A-5E 人乳腺上皮细胞激活 Fas 死亡受体,无激活组为对照。2. 分别用 NP-40(不含 SDS 和脱氧胆酸盐),RIPA buffer, Laemmli(SB)样品缓冲液提取蛋白。3. WB 进行 Clv-caspase-8 检测, Hsp90,Tubulin,P38 作为对照。■ 主要发现结果显示,仅在 Laemmli 缓冲液提取的样品中检测到激活
(无)条带,如抗体无专一性则条带无变化举个例子,癌症免疫常用的 PD-L1 抗体,下图可看到 GTX104763 PD-L1 抗体,使用基因敲弱的细胞裂解液,WB 的条带会随之变弱,显示 GTX104763 抗体具有高特异性。GTX104763 还适合多种应用,包括 WB、ICC/IF、IHC-P(可达 1:1,000)、 IHC-Fr(可达 1:1,000),及多篇文献引用,为高敏、高特异性的可靠抗体工具。又如白血病标记物-CD44,CD44 参与介导细胞存活的迁移、增殖、分化和信号传导途径。GTX
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