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 | Mapping Causal Variants with Single-Nucleotide Resolution Reveals Biochemical Drivers of Phenotypic Change |
Citation | Cell 2018. |
Authors | She, R., & Jarosz, D. F. (2018). |
Title | Human beta defensin-1 is involved in the susceptibility to adeno-tonsillar hypertrophy |
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Citation | Eukaryotic Microbiology 2017. |
Authors | Bharti, D., Kumar, S., & La Terza, A |
Title | Molecular structure of cyclomaltodextrinase derived from amylolytic lactic acid bacterium Enterococcus faecium K-1 and properties of recombinant enzymes expressed in Escherichia coli and Lactobacillus plantarum |
Citation | International Journal of Biological Macromolecules 2017. |
Authors | Unban, K., Kanpiengjai, A., Lumyong, S., Nguyen, T. H., Haltrich, D., & Khanongnuch, C. (2017). |
Title | Molecular genetic studies in Saudi population; identified variants from GWAS and Meta-analysis in Stroke |
Citation | Saudi Journal of Biological Sciences 2017. |
Authors | Alharbi, K. K., Khan, I. A., Alotaibi, M. A., Aloyaid, A. S., Al-Basheer, H. A., Alghamdi, N. A., ... & Al-Sulaiman, A. M. (2017). |
Title | EXPRESSION OF CHITINASE GENE FROM Bacillus Licheniformis DSM13 IN E.Coli T7 AND BIOCHEMICAL CHARACTERIZATION OF RECOMBINANT ENZYME |
Citation | Vietnam Journal of Agriculture 2017. |
Authors | Ninh Thi Phip * , Nguyen Thi Thanh Hai, Bui The Khuynh |
Title | KASPTM GENOTYPING TECHNOLOGY AND ITS USE IN GENETIC-BREEDING PROGRAMS (A STUDY OF MAIZE) |
Citation | Plant varieties studying and protection 2017. |
Authors | ???????, ?. ?., & ???????, ?. ? |
Title | Comparing Natural and Artificially Designed Bacterial Consortia as Biosensing Elements for Rapid Non- Specific Detection of Organic Pollutant through Microbial Fuel Cell |
Citation | Int. J. Electrochem. Sci 2017. |
Authors | Anam, M., Yousaf, S., Sharafat, I., Zafar, Z., Ayaz, K., & Ali, N |
Title | Low Prevalence of Ocular Chlamydia trachomatis Infection and Active Trachoma in the Western Division of Fiji |
Citation | PLoS One 2016. |
Authors | Macleod, C. K., Butcher, R., Mudaliar, U., Natutusau, K., Pavluck, A. L., Willis, R., ... & Rafai, E. |
Title | Barcode Sequencing Screen Identifies SUB1 as a Regulator of Yeast Pheromone Inducible Genes |
Citation | G3: Genes, Genomes, Genetics 2016. |
Authors | Sliva, A., Kuang, Z., Meluh, P. B., & Boeke, J. D |