- 询价
- 北京安必奇
- 0.156-10 ng/mL
- 0.094 ng/mL
- DEIA-FN1641
- 2026年07月14日
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- 文献和实验
- 技术资料
- 库存：
In Stock
- 检测范围：
0.156-10 ng/mL
- 检测方法：
Sandwich ELISA
- 应用：
Quantitative
- 样本：
serum, plasma, cell culture supernatants, tissue homogenate
- 灵敏度：
0.094 ng/mL
- 规格：
96T
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文献和实验Gene Editing in One‐Cell Embryos by Zinc‐Finger and TAL Nucleases
editing using sequence‐specific nucleases. Sequence‐specific nucleases are composed of a domain that binds to the target gene via zinc‐finger or TAL effector‐based DNA recognition motifs. The DNA binding part is fused to the nonspecific nuclease domain
technical steps to recover uPA and PAI-1 protein from archived breast cancer tissues and to quantitatively determine uPA and PAI-1 protein content in tumor tissue extracts by enzyme-linked immunosorbent assay (ELISA) are described in detail. The technical
harboring the plasmid that encodes the QSSR1 zinc finger fused to fingers 1 and 2 of the Zif268 protein and the Gal4 activation domain formed blue colonies only when mated with cells that contained the GTA and GCA reporter plasmids. This means
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