- 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.
The Genomic DNA Clean & Concentrator-10 (gDCC) is a 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.
|Applicable For||Eluted DNA is ideal for ligation, sequencing, labeling, PCR, microarray, transfection, transformation, restriction digestion procedures, and any other sensitive downstream application|
|Elution Volume||≥ 10 µl of DNA Elution Buffer|
|Purity||A260/A280 > 1.8, A260/A230 > 1.8|
|Sample Source||Enzymatic reactions or impure preparations containing genomic DNA.|
|Sample Storage||Eluted DNA can be used immediately or stored at ≤ -20°C.|
|Size Range||50 bp to 200 kb|
|Yield||Recovery of DNA ranges from 70 - 95%|
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 can I process naked DNA stored in DNA/RNA Shield?
Use the standard protocol (add 2 or 5 volumes of DNA binding buffer depending on DNA size).
Q3: What should I do if I did not add ethanol to the DNA Wash Buffer before starting?
The DNA will be eluted off the column during the wash step. 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?
Zymo Research recommends 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. Zymo Research recommends raising the starting volume to 100 µl with water to ensure optimal binding conditions.
|C1002-25||Zymo-Spin IC-XL||25 Pack||€43,00|
|C1002-50||Zymo-Spin IC-XL||50 Pack||€73,00|
|D5201-1-50||ChIP DNA Binding Buffer||50 ml||€37,00|
|C1001-50||Collection Tubes||50 Pack||€16,00|
|C1001-500||Collection Tubes||500 Pack||€53,00|
|C1001-1000||Collection Tubes||1000 Pack||€89,00|
|D4003-2-6||DNA Wash Buffer (Concentrate)||6 ml||€10,00|
|D4003-2-24||DNA Wash Buffer (Concentrate)||24 ml||€33,00|
|D3004-4-1||DNA Elution Buffer||1 ml||€12,00|
|D3004-4-4||DNA Elution Buffer||4 ml||€12,00|