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High Efficiency Magnetic Bead DNA Extraction Kits For PCR Applications
Fast and High Efficiency Magnetic Bead DNA Extraction Kit Purification Collection Kit for PCR Applications
product description:
HUACHENYANG DNA Extraction Kit provides a fast and efficient
magnetic bead method to purify and extract DNA (including genomic,
mitochondrial and viral DNA) from preserved tissues, saliva, body
fluids, as well as from oral cavity, cervix, skin cells, bacterial
cells, etc. Biological samples can be stored at room temperature
for up to 30 days in our proprietary storage buffer before
processing without significant loss of DNA yield or quality (more
than 30 days if stored frozen) No phenol/ Chloroform extraction or
alcohol precipitation yields high-quality genomic DNA within 15
minutes, with an average DNA yield of 8 μg per buccal swab.
Purified DNA, approximately 20-30 kb, suitable for downstream
applications such as PCR or other enzymatic reactions
Features:
Using silicon magnetic beads and buffer system with unique
separation function, it can quickly, highly sensitively and
efficiently extract high-purity nucleic acid from samples, and the
extracted and purified nucleic acid can be used for PCR, RT-PCR,
digestion, reverse transcription, and Southern Various common
downstream experiments such as blot, applicable specimen types:
whole blood, tissue homogenate, swab, serum, plasma,
bronchoalveolar lavage fluid, etc. Applicable extraction
instruments: most of the automatic nucleic acid extraction
instruments on the market
benefit:
1. Magnetic bead-based technology isolates genomic DNA without the
need for hazardous chemicals, centrifugation or vacuum manifolds,
phenol and ethanol precipitation.
2. Fast and efficient purification of genomic DNA from human buccal
swabs in less than 15 minutes after sample preparation and lysis.
3. Simple cleavage with proteinase K without any mechanical
cleavage.
4. Minimal RNA contamination.
5. Purified genomic DNA exhibits improved downstream performance in
applications such as PCR.
6. A kit is included for automated processing of large numbers of
samples in 96-well plates using a liquid handling robot.
model | CY-F006-22 (200 preps-saliva) |
Magnetic beads | 3×1.1mL |
Proteinase K solvent | 3×1.1mL |
Protease lyophilized powder | 3×22mg |
Reagent bottle size/volume2 | CY4/125mL |
Reagent bottle size/volume2 | Y5/15mL |
Product Instructions:
1. Before using nucleic acid extraction reagents
①. Transfer proteinase k solvent to lyophilized powder containing
proteinase k and mix well.
②Add 18ml and 42ml of absolute ethanol to CY3 and CY4 of CY-F006-10
(50preps-cells) and CY-F006-20 (50preps-saliva), stir well.
③. Add 36ml and 84ml of absolute ethanol to CY3 and CY4 of models
CY-F006-11 (100preps-cells) and CY-F006-21 (100preps-saliva) and
mix well.
2. Swab extraction steps:
① Dry swab collection, add 0.6ml CY1 solution and 10ul proteinase
K, mix well, and incubate in a 65°C air incubator for 30 minutes
(or wet collection: centrifuge the sample centrifuge tube
containing the swab and preservation solution to 12000 Transfer for
1 minute, keep the precipitate, remove the supernatant, add 0.6ml
of CY1 solution, 10ul of proteinase K, mix well, and incubate in an
air incubator at 65 degrees Celsius for 30 minutes).
②. Remove the swab and centrifuge at 12000rpm for 1 minute.
③. Remove all supernatants into new centrifuge tubes and perform
experiments.
④. Add 0.25ml of CY2 solution, 10ul of magnetic beads* (shake well
before use), mix for 12min, put it on a magnetic stand for 30s, and
blot dry.
⑤ Add 0.6ml of CY3 solution, stir for 3min, put it on a magnetic
stand for 30s, and absorb the liquid.
⑥. Add 0.6ml of CY4 solution, mix for 3min, put it on a magnetic
stand for 30s, and dry the liquid
⑦, repeat steps ②⑥
⑧ Dry at room temperature for 10-20min, add 50ul CY5 liquid for
elution, mix well, place it on a magnetic stand for 30s, and then
transfer the liquid to a new centrifuge tube
⑨, measure the outer diameter
3. Saliva Extraction Step
① Centrifuge saliva plus preservation solution at 12000rpm for 1min
② Retain the precipitate and remove the supernatant
③. Add 0.6ml of CY1 solution and 10ul of proteinase k, stir evenly,
and incubate in an air incubator at 65 degrees Celsius for 30
minutes.
④ Centrifuge at 12000rpm for 1min, take out all the supernatant
into a new centrifuge tube, add 10ul of magnetic beads and 0.25ml
of CY2, mix for 12min, and place it on a magnetic stand for 30s to
absorb the liquid.
⑤ Add 0.6ml of CY3 solution, stir for 3min, put it on a magnetic
stand for 30s, and absorb the liquid.
⑥. Add 0.6 ml of CY4 solution, mix for 3 min, place it on a
magnetic stand for 30 s, and absorb the liquid.
⑦, repeat step ⑥
⑧ Dry at room temperature for 10-20 minutes, add 50ul CY5 liquid
for elution, mix well, put it on a magnetic stand for 30s, and then
transfer the liquid to a new centrifuge tube.
⑨, measure the outer diameter
Note: To remove RNA, prepare RNaseA 10mg/ml: solvent (10mM sodium acetate: pH 5.0), boil for 15min, adjust pH 7.5 with Tris-HCl, and store at -20 degrees Celsius.
Precaution:
1. This product is only used for in vitro diagnosis.
2. The storage environment and extraction steps should be carried
out in strict accordance with the instructions in the instruction
manual.
3. If it is found that the amount is too small during the
extraction process, the sample size can be appropriately increased
or the number of extractions can be increased.
4. The extracted DNA must be fresh and tested in time.
Note: This transfer medium is intended for in vitro diagnostics and is not intended for internal or external use in humans or animals. If swallowed, it may cause a serious accident; it is irritating to eyes and skin. If splashed into eyes, rinse with water. It should be ventilated during use.