- ￥1622.83
- Merck
- PLBC02510
- 2026年03月11日
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- 详细信息
- 文献和实验
- 技术资料
- 规格：
10pk
PLBC02510密理博25mm再生纤维素膜滤器3 kDa 10个Millipore
| PBCC02510 | B5K 25MM HIGH FLUX 10PK |
| PBCC04310 | B5K 44.5MM HIGH FLUX 10PK. |
| PBCC04710 | B5K 47MM HIGH FLYX 10 PK. |
| PBCC06210 | B5K 63.5MM HIGH FLUX 10PK. |
| PBCC07610 | B5K 76MM HIGH FLUX 10PK. |
| PBCC09005 | B5K 90MM HIGH FLUX 5PK |
| PBCC15005 | B5K 150MM HIGH FLUX 5PK |
| PBGC02510 | B10K 25MM HIGH FLUX 10PK. |
| PBGC04310 | B10K 44.5MM HIGH FLUX 10PK. |
| PBGC04710 | B10K 47MM HIGH FLUX 10PK |
| PBGC06210 | B10K 63.5MM HIGH FLUX 10PK. |
| PBGC07610 | B10K 76MM HIGH FLUX 10PK. |
| PBGC09005 | B10K 90MM HIGH FLUX 5PK |
| PBGC15005 | B10K 150MM HIGH FLUX 5PK |
| PBHK02510 | B100K 25MM HIGH FLUX 10PK. |
| PBHK04310 | B100K 44.5MM HIGH FLUX 10PK. |
| PBHK04710 | B100K 47MM HIGH FLUX 10PK. |
| PBHK06210 | B100K 63.5MM HIGH FLUX 10PK. |
| PBHK07610 | B100K 76MM HIGH FLUX 10PK. |
| PBHK15005 | B100K 150MM HIGH FLUX 5 PK |
| PBMK02510 | B300K 25MM HIGH FLUX 10PK |
| PBMK04310 | B300K 44.5MM HIGH FLUX 10PK |
| PBMK04710 | B300K 47MM HIGH FLUX 10PK |
| PBMK06210 | B300K 63.5MM HIGH FLUX 10PK |
| PBMK07610 | B300K 76MM HIGH FLUX 10PK |
| PBMK09005 | B300K 90MM HIGH FLUX 5PK |
| PBMK15005 | B300K 150MM HIGH FLUX 5PK |
| PBQK02510 | B50K 25MM HIGH FLUX 10PK |
| PBQK04310 | B50K 44.5MM HIGH FLUX 10PK. |
| PBQK04710 | B50K 47MM HIGH FLUX 10PK. |
| PBQK06210 | B50K 63.5MM HIGH FLUX 10PK. |
| PBQK07610 | B50K 76MM HIGH FLUX 10PK. |
| PBQK09005 | B50K 90MM HIGH FLUX 5PK |
| PBQK15005 | B50K 150MM HIGH FLUX 5PK |
| PBTK02510 | B30K 25MM HIGH FLUX 10PK. |
| PBTK04310 | B3OK 44.5MM HIGH FLUX 10PK. |
| PBTK04710 | B30K 47MM HIGH FLUX 10PK. |
| PBTK06210 | B30K 63.5MM HIGH FLUX 10PK. |
| PBTK07610 | B30K 76MM HIGH FLUX 10PK. |
| PBTK15005 | B30K 150MM HIGH FLUX 5PK |
| PBVK02510 | B500K 25MM HIGH FLUX 10PK |
| PBVK04310 | B500K 44.5MM HIGH FLUX 10PK |
| PBVK04710 | B500K 47MM HIGH FLUX 10PK |
| PBVK06210 | B500K 63.5MM HIGH FLUX 10PK |
| PBVK07610 | B500K 76MM HIGH FLUX 10PK |
| PBVK15005 | B500K 150MM HIGH FLUX 5PK |
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文献和实验Active Motif ChIP 实验专家技术经验分享：如何判断 ChIP 成功与否？
/20 ug=0.5%）作为对照。ChIP 结束之后，将 5% Input DNA，H3K4me3 ChIP DNA 以及 IgG ChIP DNA 纯化之后都溶解到等体积的水、10 mM Tris pH 8.0 或 TE buffer 中。分别设计目的区域 A，阴性区域 B 和阳性区域 C 的引物。 引物扩增片段大小以小于超声后 DNA 大小为宜（一般设计 70～200 bp），因为扩增片段太大，上下游引物结合的模板有可能不是位于同一个 DNA 片段上，导致扩增效率较低，甚至会影响真实富集度。准备
Frozen competent E. coli cells 【Carnegie Institution of Washington】
Pipes-NaOH pH6.7 0.5M 10 mM 2 ml CaCl2 0.5M 15 mM 3 ml KCl 2M 0.25M 12
upon the dual pulldown to incorporate a third pulldown which is an iteration of the ChIP and is a pulldown for H3K27me3+ (Figure 1b). The third assay described here is the biotin-RNA pulldown of a low-copy RNA that spans the siRNA targeted promoter region
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