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MCLAB :: Products :: Real-time PCR Kits :: 2X HoTaq Real-time PCR Kit

2X HoTaq Real-time PCR Kit
2X HoTaq Real-time PCR Kit 
CAT HTP1

  25%
Weight 0.00 lbs
Price: $266.00

2X HoTaq Real-time PCR Kit
Quantity

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2X HoTaq Real-time PCR Kit
Catalog No.
Descriptions
Size
Price
Document
HTP400
Regular level of ROX, for Real-time PCR Machines ABI 7000, 7300, 7700, 7900
200 rnx, 4x1.25ml
$266.00
HTP400
HTP400LR
Low level of ROX, for Real-time PCR Machines ABI 7500, Mx 3000P, Mx 3005P
200 rnx, 4x1.25ml
$266.00
HTP400RF
HTP400RF
ROX Free, for Real-time PCR Machines BioRad iCycler MiniOpticon, Opticon 2, Chromo4, iQ5; Roche LightCycler 480; MJ Research DNA Engine Opticon 2, Chromo4; Corbett Roto-gene 3000, 6000
200 rnx, 4x1.25ml
$266.00
HTP400LR
Related Products: HTRT, HSM

For Research Use Only.

PRODUCT
This is a high performance real-time PCR reagent. It utilizes our own proprietary quantitative PCR technology.

ADVANTAGES
1. MCLAB's this product is similar to ABI's TaqMan® Universal PCR Master Mix, No AmpErase® UNG (CAT# 4324018) but priced 25% less!

2. MCLAB's 2X HotSybr PCR Reaction Mix products cuts down 1/2 total reaction time.

  • Normally the total reaction time is 4350 sec: 95°C, 10min => (95°C, 15sec => 60°60sec) x 50
  • For MCLAB's 2X HotSybr PCR Reaction Mix, the total reaction time is reduced to 2350 sec: 95°C, 10min => (95°C, 5sec => 60°, 30sec) x 50

3. MCLAB's One-step RT-PCR products are faster.


4. MCLAB's 2X HoTaq PCR Reaction Mix products are superior in amplifying difficult templates.
  • This is the amplification of GPIIB gene (70% G+C) .
  • 10 ~ 10K copies from 30pg human genomic DNA have been detected.


Applications
Probe based quantitative PCR including DNA quantification, 2-step RT PCR, SNP analysis, etc.

Primer and probe design
To achieve the best performance, appropriate software, such as ABI Primer ExpressTM, should be used.
    1.Tm: 60oC for primers and 68oC~70oC for probes with 17~30 nucleotides in length
    2.Amplicon size should be small, <150bp
    3.To avoid secondary structures in primers and probes
    4.To avoid more than 3 consecutive Gs in primers and probes
    5.Primers should not have complementary 3’ ends
    6.17 ~ 30 nucleotide in length
Recommended reaction conditions:
95oC, 10min. -> (95oC, 5sec. -> 60oC, 30sec.) for 50 cycles.

Recommended storage condition
-20oC

Notes
To achieve accurate quantification, it is highly recommended to do replicates. Also it is important to reduce pipetting error.

Reference
  • Holland, P. M., Abramson, R. D., Watson, R., and Gelfand, D. H. 1991. Proceedings of the National Academy of Sciences USA 88:7276–7280.
  • Livak, K. J., Flood, S. J. A., Marmaro, J., Giusti, W., and Deetz, K. 1995. PCR Methods and Applications 4:357–362.
  • Lee, L. G., Connell, C. R., and Bloch, W. 1993 Nucleic AcidsResearch 21:3761–3766.


FOR RESEARCH USE ONLY.
 

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