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60
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深圳子科生物科技有限公司
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| PCR试剂 | G008 | Taq DNA Polymerase | 5000u |
| G126 | Taq DNA Polymerase | 10000U | |
| G009 | Taq DNA Polymerase | 1000U(200 μl) | |
| G013 | 2X PCR Taq MasterMix | 5.0 ml (200 Rxns) | |
| G013-dye | 2X PCR Taq MasterMix with dye | 5.0 ml (200 Rxns) | |
| G472 | Safe-Green ; 2X PCR Taq MasterMix | 5.0 ml (200 Rxns) | |
| G012 | Taq Plus DNA Polymerase | 250 U (50 µl) | |
| G040 | Taq Plus DNA Polymerase | 1000U(200 µl) | |
| G014 | 2X PCR Taq Plus MasterMix | 5.0 ml (200 Rxns) | |
| G014-dye | 2X PCR Taq Plus MasterMix with dye | 5.0 ml (200 Rxns) | |
| G277 | TaqFast DNA Polymerase | 250 U (50 µl) | |
| G278 | TaqFast DNA Polymerase | 1000U(200 μl) | |
| G280 | 2X PCR TaqFast MasterMix | ||
| G280-dye | 2X PCR TaqFast MasterMix with dye | ||
| G078 | Precision ; DNA Polymerase | 500 U (100 µl) | |
| G011 | HotStart DNA Polymerase | 250 U (50 µl) | |
| G039 | HotStart DNA Polymerase | 1000U(200 µl) | |
| G010 | dNTP Mix | 250µl | |
| G128 | dNTP Mix | 500 µl | |
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文献和实验STANDARD PLANT MOLECULAR BIOLOGY PROTOCOLS
. Centrifuge for 5 min and wash pellet with 70 % EtOH 15. Dry pellet and resuspend the two tubes in a total of 50 l TE-buffer+RNase, use 2ml for a PCR, freeze the rest. MPS1 for 50 ml Stock 50 mM glucose 1M 2,5 ml 10 mM EDTA 0,5mM 1 ml
Standard Operating Procedures for T1-Phage Testing Assay
I. Introduction: This assay uses a lawn of phage-susceptible E. coli (DH10B) embedded in a layer of agarose. This top agarose lays on a bed of standard LB agar. If phage is present in a clone streaked or stamped onto the top agarose
DNA EXTRACTION FROM MICRODISSECTED PARAFFIN SECTIONS
. Day 1: DISSECTION: See photos of H&E , methyl green before dissection , and methyl green after dissection . Label the top of 0.5 ml pcr tubes, color code dot label them also. Add 15 ul of 1X PCR/PK Buffer into each tube, close caps
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