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- 规格:
100ug
本蛋白可用于ELISA,胶体金产品研发及细胞受体研究实验
Method of Production : Transient transfection in 293 cell culture
Method of Purification : Protein A affinity chromatography and SEC
Formulation: PBS pH7.4
Concentration: 2.50 mg/mL
Eedotoxin:<1EU/ug
0.2μm Filtration:Yes
表达宿主:Human Cells
纯度:> 95 % as determined by SDS-PAGE.
内毒素:<1.0 EU per μg protein as determined by the LAL method.
蛋白构建:
A DNA sequence encoding the receptor binding domain (RBD) of 2019-nCoV spike was expressed with the Fc region of mouse IgG1 at the C-terminus.
分子量:
The recombinant receptor binding domain (RBD) of 2019-nCoV spike consists of 457 amino acids and predicts a molecular mass of 51.5 kDa.

相关产品“
2019-nCov Spike protein S1(Fc Tag),
2019-nCov Spike protein S1(His Tag),
2019-nCov Spike protein S1(RBD,Fc Tag),
ACE2 protein,human,recombinant(Fc tag),
ACE2 protein,human,recombinant(His tag);
以上蛋白可以作为诊断试剂研发原料及受体研究实际使用,欢迎垂询;
针对2019-nCov S1蛋白,我们筛选到一株单抗,其与 S1 RBD有超强结合能力,即将闪亮登场,欢迎垂询预定。
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文献和实验干货 | 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 fusion proteins incorporating experimental protein domains fused to immunoglobulin Fc regions have become widely utilized in studies of protein–ligand interactions. The advantages of these systems include an inherent increase
Phos-tag Affinity Electrophoresis for Protein Kinase Profiling
Protein kinase profiling can provide a basis for understanding the molecular origins of diseases and, potentially, for developing tools for therapeutic intervention. It is therefore very important to develop advanced
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