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Drug Transporter Detection Kit Using 25-Multiplex PCR Assay

Jinsung SMR Co., Ltd Bioneer Corporation

http://www.jssmr.co.kr http://www.bioneer.co.kr

E-mail: js0228@chol.com Headquarters Seoul Office USA Bioneer, Inc. Order

90-39, Bangrim-dong, Nam-gu Gwangju 503-050, c 49-3,Munpyeong-dong, 412, 1580, DMC Hi-tech industry 1000 Atlantic Avenue, Alameda, http://www.jssmr.co.kr

Republic of Korea Daedeok-gu,Daejeon306-220, center, Sangam-dong, Mapo-gu, CA 94501 USA E-mail:js0228@chol.com

Phone:+82-62-672-7631 Korea Seoul, 121-835, Republic of Korea Toll free : 1-877-264-4300 Fax:+82-62-672-7632

Fax:+82-62-672-7632 Phone:+82-42-936-8500 Phone:+82-2-598-1094 Fax : 1-510-865-0350

Fax:+82-42-930-8600 Fax:+82-2-598-1096 E-mail:order.usa@bioneer.com







I. Introduction

We provides scientists with 25plex PCR assay kits to simultaneously amplify 5 sets of 5 genes, providing the rapid detection of mRNA expression for drug

transporter genes, including 24 drug transporter genes and one housekeeping gene; 17 ABC transporters (ABCA2, ABCA3, ABCB1, ABCB4, ABCB5, ABCC1,

ABCC2, ABCC3, ABCC4, ABCC5, ABCC6, ABCC9, ABCC10, ABCC11, ABCG1, ABCG2 and CFTR), one non-ABC transporter (MVP), 4 SLC transporters

(SLC28A1, SLC28A2, SLC29A1, SLC29A2), 2 copper transporters (SLC31A1 and ATP7B) and one house-keeping gene (GAPDH).



Drug Transporter Detection Kit Using 25-Multiplex PCR Assay was designed by Chemical-Mediated Hotstart method. The DNA polymerase is inhibited by the

pyrophospate, but activated upon pyrophosphate hydrolysis by the thermostable pyrophosphatase (Patent pending). This prevents the formation of mis-primed

products and primer-dimers during the reaction set up process resulting in improved PCR specificity.



In addition, Drug Transporter Detection Kit Using 25-Multiplex PCR Assay makes hot-start PCR simple and easy, eliminating the extra handling steps and

contamination risks associated with conventional hot-start methods.



Notice to Purchaser

This enzyme is specifically optimized for increasing base incorporation rate by inactivating 5’->3’ exonuclease activity. Therefore, this is not recommended to use

for Real Time PCR using Taqman® probe, which will be released soon.



II. Product Components

Description Number of Reactions



Drug Transporter Detection Kit Using

JS-001 a 32 reactions x 5 sets

25-Multiplex PCR Assay

aThe total Mg2+ concentration presented in the final 1 x working solution is 1.5 mM.

The total dNTP concentration presented in the final 1 x working solution is 1 mM (250 uM of each dNTP).





III. PCR Protocol using Drug Transporter Detection Kit Using 25-Multiplex PCR Assay

This protocol serves only as a guideline for PCR amplification. Optimal reaction conditions such as incubation times, temperatures, and amount of template DNA

may vary and must be individually determined.

Notes: • Each PCR program be sufficient to started an Pre-denaturation step of 5 min at 94°C.

• Set up reaction mixtures in an area separate from that used for DNA preparation or PCR product analysis.

• Use disposable tips containing hydrophobic filters to minimize cross-contamination.

1. Prepare the Drug Transporter Detection Kit Using 25-Multiplex PCR Assay and template cDNA.



2. Add template DNA (≤1,000ng/reaction) to the individual PCR tubes.

A negative control (without template DNA) should always be included. It is not necessary to keep PCR tubes on ice as nonspecific DNA synthesis cannot

occur at room temperature due to the inactive state of Hot Start DNA Polymerase.



Component Volume/reaction Final concentration

Drug Transporter Detection Kit Using 20ul 1 unit of HotStart DNA Polymerase

25-Multiplex PCR Assay 1x PCR Buffer*

250 µM of each dNTP

Template DNA

Template DNA, added in step 2 Variable 200 ~ 1,000 ng/reaction

Total volume 20 µl –

* Contains 15 mM MgCl2



3. Add distilled water to Drug Transporter Detection Kit Using 25-Multiplex PCR Assay tubes until the total volume of mixture becomes 20 l.

Dissolve the lyophilized blue pellet by vortexing and spin-down.

4. When using a thermal cycler with a heated lid, do not use mineral oil. Proceed directly to step 5. Otherwise, overlay with approximately 50 µl of

mineral oil.









V109C3 Blazing the Biotechnology Trail

Drug Transporter Detection Kit Using 25-Multiplex PCR Assay

Jinsung SMR Co., Ltd Bioneer Corporation

http://www.jssmr.co.kr http://www.bioneer.co.kr

E-mail: js0228@chol.com Headquarters Seoul Office USA Bioneer, Inc. Order

90-39, Bangrim-dong, Nam-gu Gwangju 503-050, c 49-3,Munpyeong-dong, 412, 1580, DMC Hi-tech industry 1000 Atlantic Avenue, Alameda, http://www.jssmr.co.kr

Republic of Korea Daedeok-gu,Daejeon306-220, center, Sangam-dong, Mapo-gu, CA 94501 USA E-mail:js0228@chol.com

Phone:+82-62-672-7631 Korea Seoul, 121-835, Republic of Korea Toll free : 1-877-264-4300 Fax:+82-62-672-7632

Fax:+82-62-672-7632 Phone:+82-42-936-8500 Phone:+82-2-598-1094 Fax : 1-510-865-0350

Fax:+82-42-930-8600 Fax:+82-2-598-1096 E-mail:order.usa@bioneer.com



5. Program the thermal cycler according to the manufacturer’s instructions.

Each PCR program is equal to Pre-denaturation step at 94°C for 5 min. A typical PCR cycling program is outlined below.



Time Temperature Additional comments

Pre-denaturation step: 5 min 94°C Equal to General PCR’s Initial activation step



Denaturation 30sec 94°C



3-step cycling Annealing 30sec 57°C



Extension 30sec 72°C

Number of cycles: 35

Final extension: 5 min 72°C



6. Place the PCR tubes in the thermal cycler and start the cycling program.

Note: After amplification, samples can be stored overnight at 2–8°C or at –20°C for longer storage.



7. Load 5ul ~ 10ul of samples on agarose gel without adding loading dye mixture and perform 2.0% agarose gel electrophoresis.









Ordering Information



Tube type Reaction Cat.No. Description

0.2 ml Tube 20 ul JS-001 0.2 ml thin-wall 8-strip tubes with attached cap / 32 tubes x 5 sets









V109C3 Blazing the Biotechnology Trail



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