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- 详细信息
- 文献和实验
- 技术资料
- 抗体名:
ALRH; BHR1; MGC116786; MGC116788; MGC116789; P600; Interleukin-13
- 抗体英文名:
ALRH; BHR1; MGC116786; MGC116788; MGC116789; P600; Interleukin-13
- 靶点:
-
- 浓度:
>95% by SDS-PAGE
- 应用范围:
-
- 宿主:
Cynomolgus
- 适应物种:
-
- 保质期:
Within 1 week, 2 to 8 °C under sterile conditions after reconstitution. 12 months from date of receipt, -20 to -80 °C as supplied. Avoid repeated freeze-thaw cycles.
- 抗原来源:
-
- 目录编号:
-
- 级别:
-
- 库存:
现货
- 供应商:
爱必信(上海)生物科技有限公司
- 标记物:
-
- 克隆性:
-
- 保存条件:
Within 1 week, 2 to 8 °C under sterile conditions after reconstitution. 12 months from date of receipt, -20 to -80 °C as supplied. Avoid repeated freeze-thaw cycles.
- 形态:
Lyophilized Powder
- 亚型:
-
- 免疫原:
-
- 规格:
10ug/50ug
| 规格: | 10ug | 产品价格: | ¥906.0 |
|---|---|---|---|
| 规格: | 50ug | 产品价格: | ¥2970.0 |
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文献和实验One-Step Purification of Recombinant Proteins with the 6xHis Tag and Ni-NTA Resin
The 6xHis/Ni-NTA system is a fast and versatile tool for the affinity purification of recombinant proteins and antigenic peptides. It is based on the high-affinity binding of six consecutive histidine residues (the 6xHis tag) to immobilized
干货 | CUT and Tag 核心酶 Hyperactive PA/PG-Tn5 Transposase 大解密
CUT&Tag(Cleavage Under Targets and Tagmentation)是蛋白-DNA 互作的一大革新技术,它不需要使用甲醛交联以及免疫共沉淀,而是通过针对靶蛋白(如转录因子、染色质重塑蛋白)的抗体和 Protein A/G 的介导,使得与 Protein A/G 融合的 Tn5 酶(Tagmentase)在切割 DNA 片段的同时在序列两端加上测序接头,经 PCR 扩增后即可形成用于高通量测序的文库(见图 1 )。CUT &Tag 技术具有细胞投入量低、信噪
Recombinant DNA Engineering, Or Cloning Genes In Plasmids
and thus fusion proteins. For example there might be sequence for a fluorescent protein such as GFP or a peptide tag such as HA upstream of MCS (and downstream of promoter) so that an insert in frame will lead to the generation of a fusion protein, an N-terminal
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