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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 保存条件:
常温
- 英文名:
Genomic DNA Clean & Concentrator-25
- 供应商:
简石生物
HIGHLIGHTS
- Quick (5 minute) clean-up of large-sized DNA from any enzymatic reaction or impure preparation without messy precipitations
- Unique spin column for low volume elution of ultra-pure, high-yield DNA
- Eluted DNA is ideal for PCR, endonuclease digestion, sequencing, etc.
DESCRIPTION
The Genomic DNA Clean & Concentrator-25 (DCC) is a spin column gDNA clean up kit that provides quick (5 minute) recovery of ultra-pure, large-sized DNA (e.g., genomic, mitochondrial, plasmid (BAC/PAC), viral, phage, (wga) DNA, etc.) from any enzymatic reaction or impure preparation (e.g., Proteinase K digestion). There is no need for organic denaturants, chloroform, or messy precipitations: simply add the specially formulated ChIP DNA Binding Buffer to a sample and then transfer the mixture to the supplied Zymo-Spin Column. Eluted DNA is suitable for sequencing, PCR, endonuclease digestion, and other enzymatic procedures. This gDNA clean up kit is also compatible with smaller DNAs (50 bp to 10 kb) from PCR, digestions, crude plasmid preparations, cDNA synthesis, etc.
| DNA Recovery | Typically, up to 25 µg total DNA per column can be eluted into ≥35 µl of low salt DNA Elution Buffer or water. |
|---|---|
| DNA Size Limits | Capable of purifying small DNA fragments > 50 bp and large sized DNAs up to 200 kb. |
| Sample Sources | DNA from impure preparations of genomic DNA (e.g., Proteinase K digestions), plasmid DNA (including BAC), viral DNA, and whole genome amplified (wga) DNA. Can also be used for the purification of low molecular weight DNA (50 bp to 10 kb) from PCR, endonuclease digestion, post-RT cDNA synthesis, etc.. |
| DNA Purity | High-quality (A(260/280) ≥ 1.8) high molecular weight DNA ideal for ligation, sequencing, labeling, PCR, microarray, transfection, transformation, and restriction digestion procedures. |
| Product Detergent Tolerance | ≤5% Triton X-100, ≤5% Tween-20, ≤5% Sarkosyl, ≤1% SDS. |
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文献和实验Clean-up Spin Protocol For DNA fragments (30bp-100 bp) 1) Add 3 x volume of buffer P3, 3 x volume of isopropanol to the enzymatic reaction and mix throughly with pipetting or vortex. The maximum volume of the reaction can be processed
A protocol for cleaning and reusing the large 25 x 25 cm plates
We regularly reuse our large 25x25 cm plating trays; initially, however, we were plagued by gross microbiological contamination when reusing the trays. Various combinations of cleaning with a laboratory dishwasher, ethyl alcohol, and UV
for downstream digests oheat 5 minutes at 60 degrees ospin 2 min @ full speed in microcentrifuge oremove DNA-containing supernatant to clean tube Notes & Misc: •Conveinient PCR clean up before digestion: 100μl PCR reaction cleaned up with 50μl silica











