- 询价
- KERAFAST
- EMB005
- 2026年04月08日
企业认证
相关产品推荐更多 >
万千商家帮你免费找货
0 人在求购买到急需产品
- 详细信息
- 文献和实验
- 技术资料
风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
文献和实验Non-fluorescent protein/RNA double-labeling
, 50 ug/ml heparin, and 250 ug/ml tRNA). You can also include 1% BSA providing you know it is ultra pure/RNase-free. With our reagents, we find we get similar results without it. 4. Incubate with the primary antibody (diluted appropriately in PBTH
Non-fluorescent protein/RNA double-labeling
Non-fluorescent protein/RNA double-labeling (a version of this is described in: Manoukian, A. and Krause, H.M.(1992) Genes Dev ., 6: 1740-1751.) 1. Collect embryos, dechorionate and fix in a (1:1) mixture of heptane:fix. Fix
by reaction with alkaline phosphatase-conjugated goat anti-mouse secondary antibody. Choose the actin pool broadly, however, consider also checking the column fractions by dot blot with mAB 3F2 to identify capping protein. Pool the actin fractions
技术资料暂无技术资料 索取技术资料
