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- 详细信息
- 文献和实验
- 技术资料
- 保质期:
1年
- 英文名:
In-Fusion™ Dry-Down PCR Cloning Kit w/Cloning Enhancer
- 供应商:
北京智杰方远
- 保存条件:
-20度
- 规格:
24 rxns
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文献和实验Inverse PCR & Cycle Sequencing
) 2.0ul 1) Incubate O/N at 4°. 2) Ethanol precipitate on ice, 10min. 3) Spin, aspirate, pulse, aspirate. 4) Speed Vac briefly to dry pellet. 5) Resuspend in 150ul TE (~1/150 fly per ul). IV. PCR Set up PCR reactions
DETECTION OF ß-GALACTOSIDASE AND ALKALINE PHOSPHATASE ACTIVITIES IN TISSUE
background. 4. Incubate tissue in X-Phos/NBT Detection Buffer for 15' at room temperature. XPhos/NBT Detection Buffer (Buffer 3 as described for Genius kit by Boehringer-Mannheim) 100 mM Tris-HCl, pH 9.5 100 mM NaCl 50 mM MgCl
Replication timing by density transfer
-Aldrich (previously from Isotec, which is now part of Sigma-Aldrich) "-N" medium =1.61 g yeast nitrogen base w/o amino acids and ammonium sulfate, 11.1 g succinic acid, 6.67 g NaOH per litre. Pronase : We use
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