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- 详细信息
- 文献和实验
- 技术资料
- 库存:
大量
- 保修期:
一年
- 现货状态:
现货
- 供应商:
科邦兴业(北京)科技有限公司
- 规格:
盒
sartorius赛多利斯11406--25------NCN white - black, non-sterile, 0.45 µm
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文献和实验In Situ Hybridization Using Digoxigenin Labeled Probes
as black bands. Weaker signals are brown Solutions: 1) 10X PBS 1.3 M NaCl 0.07 M Na2HPO4 0.03 M NaH2PO4 2) Hybridization Buffer 0.6 M NaCl 50 mM Sodium phosphate buffer, pH 6.8 1X Denhardt's (0.02% BSA / 0.02% Ficoll / 0.02
Construction and Characterization of Adenovirus Vectors
), 1.25 g/mL and 1.35 g/mL, in dialysis buffer Prepare each gradient solution separately. Sterilize by filtration through a 0.2-µm filter. Chloroform:isoamyl alcohol (24:1) Citric saline (2X) For 1X citric saline, dilute the 2X
Methods for the preparation of Fly Extract (FE1 and FE2).
you may have to filter through 0.8µm and 0.45µm filters first. Aliquot to 2.5ml and freeze at -20°C. Fly Extract 1 for initiating primary culture (FE1) 1. Procedure as for FE2 but the flies
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