Genomic DNA Isolation Kit
For the isolation of genomic DNA from animal tissues, cells, bodily fluids, virus and swabs
For research use only and NOT intended for in vitro diagnostics.
Genomic DNA Isolation Kit
For the isolation of genomic DNA from animal tissues, cells, bodily fluids, virus and swabs
Register today to receive an exclusive 15% off* on your first order.
Features and Benefits
- Isolate genomic DNA from animal tissues, cells, bodily fluids, viruses and swabs
- Rapid and convenient spin column procedure
- Purified DNA is of the highest quality and integrity for sensitive downstream applications including PCR, qPCR, genotyping, sequencing and more
This kit is designed for the rapid preparation of genomic DNA from various tissue samples, cultured cells, viruses, bodily fluids and swabs using a rapid spin column protocol. Purified DNA is of an excellent yield and quality, and is immediately ready for any downstream application including PCR, qPCR, genotyping, sequencing and more. The protocol can be completed in approximately 80 minutes (including incubation time).
Details
Supporting Data
Kit Specifications
|
|
Column Binding Capacity |
25 µg
|
Average Yield:* HeLa Cells (1 x 106) Tissue (from 10 mg kidney) |
8 µg 10 µg |
Maximum Amount of Starting Material: Animal Tissues Cultured Cells Bodily Fluids (blood, saliva) Viral Suspension |
20 mg 3 x 106 cells 150 µL 150 µL |
Time to Complete 10 Purifications |
80 minutes
|
* Yield will vary depending on the type of sample processed
Storage Conditions and Product Stability
The Proteinase K should be stored at -20°C upon arrival and after reconstitution. All other solutions should be kept tightly sealed and stored at room temperature. This kit is stable for 2 years after the date of shipment.
Component | Cat. 24700 (50 preps) | Cat. 24750 (100 preps) | Cat. 24770 (250 preps) |
---|---|---|---|
Digestion Buffer A | 25 mL | 2 x 25 mL | 5 x 25 mL |
Buffer SK | 30 mL | 2 x 30 mL | 5 x 30 mL |
Wash Solution A | 18 mL | 2 x 18 mL | 5 x 18 mL |
Elution Buffer B | 30 mL | 2 x 30 mL | 5 x 30 mL |
Proteinase K | 12 mg | 2 x 12 mg | 5 x 12 mg |
Spin Columns | 50 | 100 | 250 |
Collection Tubes | 50 | 100 | 250 |
Elution Tubes (1.7 mL) | 50 | 100 | 250 |
Product Insert | 1 | 1 | 1 |
Documentation
FAQs
Spin Column
Column clogging may occur due to the sample being too large. Do not exceed the recommended amount of starting materials. The amount of starting material may need to be decreased if the column shows clogging below the recommended levels. Clogging can also be alleviated by increasing the g-force and/or centrifuging for a longer period of time until the lysate passes through the column.
Lysate can be more gelatinous prior to loading onto the column due to the following factors:
- The lysate solution mixture is not homogeneous. To ensure a homogeneous solution, vortex for 10-15 seconds before applying the lysate to the spin column.
- Maximum number of cells or amount of tissue exceeds kit specifications. Refer to specifications to determine if the amount of starting material falls within kit specifications.
A low genomic DNA yield may be caused by:
- Improper storage of samples. Tissue samples and cell pellets may be frozen and stored at -20°C or -70°C. Repeated freezing and thawing of stored samples should be avoided, as this may lead to decreased yields of DNA.
- Incomplete lysis of cells. Extend the incubation time of Proteinase K digestion or reduce the amount of tissue or cells used for lysis.
- The DNA elution is incomplete. Ensure that centrifugation at 14,000 x g is performed after the 3,000 x g centrifugation cycle, to ensure that all the DNA is eluted.
Shearing of genomic DNA can be due to the following reasons:
- The genomic DNA was handled improperly. Pipetting steps should be handled as gently as possible. Reduce vortexing times during mixing steps (no more than 10-15 seconds).
- Improper storage of sample. Repeated freezing and thawing of stored samples should be avoided as this may lead to decreased DNA size.
- The sample is old. Sheared DNA may be obtained from old tissue or cell samples. Fresh samples are recommended for maximum genomic DNA yield.
Yes, mitochondrial DNA (mtDNA) can be successfully isolated using this kit. Please contact our Tech support team at support@norgenbiotek.com and ask for reference publications.
Citations
Title | Lack of association between UBE2E2 gene polymorphism (rs7612463) and type 2 diabetes mellitus in a Saudi population |
Citation | Acta Biochimica Polonica 2014. |
Authors | KK Alharbi, IA Khan, YA Al-Sheikh, FK Alharbi, FK Alharbi, MS Al-Nbaheen |
Title | Overexpression of D-Xylose Reductase (xyl1) Gene and Antisense Inhibition of D-Xylulokinase (xyiH) Gene Increase Xylitol Production in Trichoderma reesei |
Citation | BioMed Research International 2014. |
Authors | Y Hong, M Dashtban, G Kepka, S Chen, W Qin |
Title | RNF8-Independent Lys63 Poly-Ubiquitylation Prevents Genomic Instability in Response to Replication Associated DNA Damage |
Citation | PLoS One 2014. |
Authors | C Ramaekers, T van den Beucken, RG Bristow, RK Chiu, D Durocher, BG Wouters |
Title | Retrotransposon Hypomethylation in Melanoma and Expression of a Placenta-Specific Gene |
Citation | PLoS One 2014. |
Authors | EC Macaulay, HE Roberts, X Cheng, AR Jeffs, BC Baguley, I'm Morison |
Title | Clonal architecture of chronic myelomonocytic leukemias |
Citation | Blood 2013. |
Authors | Raphael Itzykson, Olivier Kosmider, Aline Renneville, Margot Morabito, Claude Preudhomme, Celine Berthon, Lionel Ades, Pierre Fenaux, Uwe Platzbecker, Olivier Gagey, Phillipe Rameau, Guillaume Vainchenker, Nathalie Droin, Eric Solary |
Title | Polymorphic variants of MnSOD Val16Ala, CAT-262 C<T and GPx1 Pro198Leu genotypes and the risk of laryngeal cancer in a smoking population |
Citation | The Journal of Laryngology & Otology 2013. |
Authors | G Aynali, M Dogan, R Sutcu, O Yuksel, M Yariktas, F Unal, H Yasan, B Ceyhan, M Tuz |
Title | Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements |
Citation | American Journal of Human Genetics 2013. |
Authors | E Grundberg, E Meduri, JK Sandling, AK Hedman, S Keildson, A Biul, S Busche, W Yuan, J Nisbet, M Sekowska, Wilk, A Barrett, KS Small, B Ge, M Caron, SY Shin, M Lathrop, ET Dermitzakis, ML McCarthy, TD Spector, JT Bell, P Deloukas |
Title | Association of angiotensin converting enzyme gene insertion/deletion polymorphism and familial hypercholesterolemia in the Saudi population |
Citation | Lipids in Health and Disease 2013. |
Authors | KK Alharbi, TS Kashour, W Al-Hussaini, MS Al-Nbaheen, S Mohamed, RMW Hasanato, W Tamimi, MY Al-Naami, IA Khan |
Title | Association of azoospermia factor region deletions in infertile male subjects among Malaysians |
Citation | Andrologia 2013. |
Authors | AA Hussein, R Vasudevan, I Patimah, N Prashant, FA Nora |
Title | Developing a rapid, efficient and low cost method for rapid DNA extraction from arthropods |
Citation | Ciencia Rural, Santa Maria 2011. |
Authors | Nicolas Oliveira Mega, Luis Fernando Revers |