- \粪便收集\
- Quick-DNA Fungal/Bacterial Kits
- 快速DNA试剂盒
- \Select-a-Size DNA干净
- \Zymoclean DNA凝胶回收试剂盒\
- \Zymoprep酵母质粒Miniprep包\
- <我>混合
- 组织收集的
- \Direct-zol RNA包\
- \向量集合和环境\
- \XJ自我分解<我> E。"},{"src":"coli<\/i> strains","tgt":"杆菌< \/ i >菌株的
- \<我> < \/ i >快速dna植物\/种子包
- 血液采集的
- \<我> < \/ i >快速dna真菌\/细菌板\
- \基因组DNA干净
- 尿液收集的
- 混合和去活性细胞
- Quick-DNA Plant/Seed Kits
- \除OneStep PCR抑制剂包\
- \<我> < \/ i >快速dna粪便\/土壤微生物板\
- \DNA干净
Highlights
- Quick (20 minute), large-scale recovery of ultra-pure DNA from PCR, endonuclease digestions, cell-free lysates, etc.
- ZR-96 Silicon-A Plate design allows DNA to be eluted at high concentrations into minimal volumes of solvent.
- Eluted DNA is well suited for use in PCR, DNA sequencing, DNA ligation, endonuclease digestion, RNA transcription, radiolabeling, etc.
Description
| Detergent Tolerance | ≤5% Triton X-100, ≤5% Tween-20, ≤5% Sarkosyl, ≤0.1% SDS |
|---|---|
| Elution Volume | ≥ 30 µl for shallow well, ≥ 10 µl for deep well |
| Equipment | Centrifuge with microplate carriers |
| Purity | A260/A280 > 1.8 |
| Sample Source | DNA from PCR, endonuclease digestions, DNA modification reactions, isotope/fluorescence labeling reactions, etc. |
| Size Range | 75 bp to 23 kb for shallow well, 50 bp to 23 kb for deep well |
| Yield | ≤ 5 µg total DNA can be recovered.For DNA 75 bp to 10 kb the recovery is 70-90%. For DNA 11 kb to 23 kb the recovery is 50-70%. |
Q1: What is the lower limit and minimal amount of DNA that can be recovered?
Picogram levels of DNA can be recovered. The limitation is based on sensitivity of detection method.
Q2: How to process naked DNA stored in DNA/RNA Shield?
Add an equal volume of ethanol (95-100%) to the sample and mix well. The sample is ready-to-bind and does not require DNA Binding Buffer. Proceed to Step 2.
Q3: What to do if ethanol addition to the DNA Wash Buffer was omitted?
The DNA will be eluted off the column. Rebind samples using the appropriate amount of DNA Binding Buffer and wash the column with the properly prepared wash buffer.
Q4: What happens if more DNA was loaded on the columns than the stated maximum binding capacity?
Oversaturation of the column can result in total DNA loss due to clogging of silica matrix.
Q5: How many times can columns be reloaded?
We recommend no more than 5 times as binding efficiency might decrease.
Q6: What is the minimum input volume of DNA sample?
Working with volumes below 50 µl can result in decreased recovery. We recommend raising the starting volume to 100 µl with water to ensure optimal binding conditions.
| Cat # | Name | Size | Price | |
|---|---|---|---|---|
| D4003-2-24 | DNA Wash Buffer (Concentrate) | 24 ml | $33.00 | |
| D4004-1-L | DNA Binding Buffer | 100 ml | $57.00 | |
| D4003-2-48 | DNA Wash Buffer (Concentrate) | 48 ml | $60.00 | |
| C2001 | Silicon-A Plate | 2 Plates | $129.00 | |
| C2003 | Elution Plate | 2 Plates | $19.00 | |
| C2002 | Collection Plate | 2 Plates | $22.00 |
