Home  |  Contact Us   |  Blog
Toll Free North America:
1 (866) 813-6354
Direct Line:
1 (613) 723-5757
The first synthetic human chromosome was constructed by US scientists in 1997.
Collection
Q.
What is the DNA yield?
A.
From a study of 208 samples, the median amount of DNA was 110 ug per 2 mL of saliva, and the average was 100 ug. The 25% percentile was 62 ug and the 75% percentile was 158 ug. The range was 10 to 375 ug. Click here for the complete whitepaper.
Q.
What is the best way to quantify my DNA yield?
A.
We recommend quantifying your DNA with a fluorescent dye such as SYBR Green or PicoGreen (Molecular Probes) because these dyes bind to double-stranded DNA. Quantification by absorbance will tend to over-estimate the amount of DNA because of absorbance by RNA co-purified with the DNA. For more details, please consult our quantification protocols DNA Quantification using the Rotor-Gene Real Time PCR Instrument or DNA Quantification using SYBR Green I Dye and Micro-Plate Reader.
Q.
The median yield of my Oragene•DNA samples is lower than 110 ug. Why is this?
A.
There is a degree of variability in the amount of DNA in saliva. Even in the same donor, the amount of DNA in saliva can vary from day to day. Additionally, the total DNA yield can vary depending on the method of purification used. The amount of DNA found in some Oragene DNA/saliva samples may exceed the binding capacity of some column and bead-based purification kits; in these cases, not all the DNA in the sample will be recovered and the median yields will appear to be lower. Typically, the manual method of purification will recover all of the DNA in the sample.
Q.
What can I do to increase the yield of DNA?
A.
Low yields often result from samples containing less than 2 mL of saliva. To optimize DNA yields ensure your donors spit the full 2 mL of saliva as indicated in the user instructions. Click here for the complete whitepaper.
Q.
Does the Oragene•DNA kit still work if someone spits more or less than 2 mL of saliva?
A.
Yes, the Oragene•DNA chemistry can handle variability in saliva volumes from 1.5 to 2.5 mL.
Q.
What is the source of the DNA in saliva?
A.
Q.
How can I collect saliva from infants and young children who cannot spit?
A.
Please consult our protocol for "Using Saliva Sponges to Collect DNA samples from Infants & Young Children" for more information.
Q.
How can I collect saliva from dogs, cows, horses, and other animals?
A.
DNA samples can be easily collected from companion animals such as dogs, cats, laboratory animals and wildlife with the Oragene•ANIMAL product line. Click here for more information.
Q.
How can I collect DNA from cattle, pigs, sheep and other livestock animals?
A.
DNA samples can be easily collected from livestock with the Performagene•LIVESTOCK product line. Click here for more information.
Q.
How much bacterial DNA is in my Oragene•DNA samples?
A.
Using a real-time PCR assay with bacterial 16S rRNA primers, the median amount of bacterial DNA was 6.8%, with a range from 2 to 29%. In comparison, DNA collected with mouthwash contains about 50% bacterial DNA and buccal swabs may be almost 90% bacterial. The small amount of bacterial DNA content in Oragene•DNA does not affect downstream applications. Click here for the complete whitepaper.
Q.
Do you have any recommendations on how to conduct a mailing study with the Oragene•DNA kits?
A.
Yes, please consult our Mailing Recommendations.
Storage
Q.
What temperature should I store my saliva samples in Oragene•DNA?
A.
Oragene•DNA stabilizes the DNA in saliva across a range of temperatures. Saliva samples may be stored at room temperature or frozen at temperatures such as -20°C or
-80°C, depending on which is most convenient for you. Please note that storage at 4°C is not recommended for Oragene samples. Consult our "DNA Stability with Oragene•DNA" application note for more details.
Q.
Can saliva samples in Oragene•DNA frozen and then thawed?
A.
Yes, saliva samples may undergo at least five freeze-thaw cycles with no evidence of DNA degradation. Please consult our "Long-term Storage Recommendations" application note for more details.
Purification
Q.
The A260/280 ratio of my purified DNA is low. What can I do to improve this?
A.

DNA from saliva purified with the Oragene•DNA ethanol precipitation protocol should have A260/280 ratios ranging from 1.6 to 1.9. If your ratio is low, try the following trouble-shooting tips:

  1. check that the Oragene•DNA samples have been incubated for at least 1 hour at 50°C before purification,
  2. when purifying the Oragene•DNA sample, be sure not to disturb the protein pellet after the first centrifugation step,
  3. check that your spectrophotometer is subtracting the A320 value from the A260 and A280 values (A320 represents the background turbidity of the sample), and
  4. check that the individual A260 and A280 values are in the range from 0.1 to 1.0 (i.e. within the linear range of the spectrophotometer).

Please see our white paper entitled "From turbidity to clarity: Simple methods to improve the A260/A280 ratio of Oragene®•DNA purified DNA samples" for more information.

Q.
Can saliva samples stored in Oragene•DNA be purified using methods other than the ethanol precipitation protocol supplied with the kit?
A.
Yes, homebrew methods such as phenol/chloroform extraction or commercial kits such as QIAamp (Qiagen) and PUREGENE (Gentra) may be used to purify DNA from Oragene•DNA samples. Please see our purification application notes for more information.
Q.
Can saliva samples stored in Oragene•DNA be purified using automated DNA extraction robots?
A.
Yes, DNA from Oragene•DNA samples have been purified using robots such as the BioRobot EZ1 (Qiagen), AutoPure (Gentra), Magtration 12GC (PSS Bio), Tecan, Biomek NX/FX, among others. Please see our purification application notes for more information.
Q.
When I run an agarose gel on my purified DNA, there is a large smear at the bottom of the gel. Is this degraded DNA?
A.
No, the smear is low molecular weight RNA.
Q.
How can I remove the RNA from my samples?
A.
Please consult our protocol "RNA removal by double-RNase digestion" for more information.
Downstream Applications
Q.
Which downstream applications are compatible with DNA from Oragene•DNA?
A.
DNA from Oragene•DNA is fully functional with PCR, real-time PCR, multiplex PCR, SNP genotyping, microarrays, sequencing, RFLP, etc. Please see our application notes for more information.
Q.
Can Whole Genome Amplification (WGA) be performed on DNA from Oragene•DNA?
A.
Yes, DNA from Oragene•DNA can be used as the template for commercially-available WGA kits such as GenomiPhi (GE Healthcare), GenomePlex (Sigma-Aldrich), and REPLI-g (Qiagen).
Q.
Does the bacterial DNA in Oragene•DNA samples interfere with downstream applications?
A.
DNA from Oragene•DNA performs the same as DNA from blood for downstream applications because the amount of bacterial DNA in Oragene•DNA samples is low, and PCR-based technologies have good specificity. For your interest, our application note entitled "SNP genotyping of Oragene•DNA™ with SNP stream®" shows that the SNP genotyping calls are identical with DNA from blood versus DNA from Oragene•DNA. Additionally, Affymetrix has published a technical note (link: http://www.affymetrix.com/support/technical/technotes/saliva_gDNA_genotyping.pdf) showing that the performance of DNA from Oragene DNA/saliva samples is identical to that of DNA from blood in SNP microarray applications.
Q.
Do you have any recommendations for using DNA from Oragene•DNA with Affymetrix or Illumina chips?
A.
Yes, for Affymetrix or Illumina chips, we recommend purifying the Oragene•DNA samples using the Oragene Manual Purification Method with the following modifications:
  1. Dissolve the final DNA pellet in 50 uL of water or TE buffer instead of the 100 uL suggested in the protocol. This will help ensure that the DNA concentration is suitable for use on microarrays.

Additionally, the purified DNA MUST be quantified using a fluorescent method such as Sybr Green or Picogreen. See our DNA Quantification protocols for more information.

 
"I found the Oragene•DNA collection kit very simple to use. The protocol was easy to follow and time-saving permitting me to perform the extraction amplification and analysis steps in a single day."

Melissa Boweman, Technologist
Plexagen Diagnostics Ltd.

© 2010 DNA Genotek Inc.