KOD -Multi & Epi-, Trial (Only 1 Per Customer)

Product#: TYB-KME-101S
$1.00

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TOYOBO · Diagnocine

KOD -Multi & Epi-, Trial (Only 1 Per Customer)

DESCRIPTIONKOD -Multi & Epi- is a high-fidelity PCR enzyme based on genetically modified KOD DNA polymerase(UKOD). This modified enzyme enables amplification from templates containing uracils (U) or using primers containing inosines (I)…

Cat No.
TYB-KME-101S
UNSPSC Code
12352204
Packaging
1 vial
Storage Temp.
-20°C  | Ships on Dry Ice

Shipping & ordering notice: This product has ICE or DRY ICE shipping requirements, DO NOT select Ground Shipping. $1.00 is only for sample (please inquire)

Product Overview

KOD -Multi & Epi- (*Only 1 Per Customer*)

Cat No. List & Ordering
Product Name Cat. No. Size Storage Order
KOD -Multi & Epi-, Trial TYB-KME-101S 1 vial Store at -20°C ( 4°C for a month ) Current page
KOD -Multi & Epi-, 1 pack TYB-KME-101 200 µl X 1 Store at -20°C ( 4°C for a month ) Order
KOD -Multi & Epi-, 5 pack TYB-KME-101-5PK 200 µl X 5 Store at -20°C ( 4°C for a month ) Order
KOD -Multi & Epi-, 10 pack TYB-KME-101-10PK 200 µl X 10 Store at -20°C ( 4°C for a month ) Order
DESCRIPTION
KOD -Multi & Epi- is a high-fidelity PCR enzyme based on genetically modified KOD DNA polymerase(UKOD). This modified enzyme enables amplification from templates containing uracils (U) or using primers containing inosines (I) and uracils (U). Furthermore, addition of the Elongation Accelerator significantly reduces amplification bias during PCR. KOD -Multi & Epi- can be applied to various purposes such as a) multiplex PCR, b) bisulfite PCR in epigenetics research, and c) metagenomics research.
 
This enzyme is also applicable for the preparation of DNA fragments for next-generation sequencing and capillary sequencing via cloning because the enzyme exhibits about 11-fold higher PCR fidelity.
 
KOD -Multi & Epi- contains two types of anti-KOD DNA polymerase antibodies that inhibit the polymerase and its 3'→5' exonuclease activity, thus allowing for Hot Start PCR. Furthermore, KOD -Multi & Epi- generates blunt-end PCR products because of its 3'→5' exonuclease (proof-reading) activity.

FEATURES

 

  • Homogeneous amplification (Low bias)
  • Effective amplification from templates containing uracils (U) and primers containing uracil (U) or Inosine (I) can be used
  • High fidelity
  • Applicable for amplification from crude samples
  • Highly efficiency
     

APPLICATIONS
KME-101_application.png

SOURCE
E. colistrain carrying the cloned KOD DNA polymerase gene
 
COMPONENTS
KOD -Multi & Epi-® (1.0 U/uL)* 200 uL × 1
2× PCR Buffer for KOD -Multi & Epi-** 1.7 ml × 3
*The enzyme solution contains anti-KOD DNA polymerase antibodies that neutralize the polymerase and inhibit its 3'→5' exonuclease activities.
**The 2× PCR Buffer for KOD -Multi & Epi- contains dNTPs (dATP, dGTP, dCTP and dTTP), and Mg2+ at 4.0 mM (final concentration: 2.0 mM).
 
APPLICATION DATA
Example 1.PCR performance in Multiplex PCR
The small targets from 200 to 1,000 bp and the large target from 1 to 10 kb were amplified by single-plex or multiplex PCR. Each target was successfully amplified by both single-plex and multiplex PCR.

KME-101_example1-1.png
M:100 bp DNA ladder
1:DDB2 200 bp
2:FANCG 250 bp
3:HBg 300 bp
4:CDH1 400 bp
5:chrome9 500 bp

6:ERCC4 550 bp
7:HRAS 600 bp
8:PRF1 700 bp
9:BRCA1 800 bp
10:CDK4 1000 bp
MP:Multiplex PCR 1~10
Sample
Human genomic DNA 50ng
Primer concentration
0.3mM each
Multiplex PCR cycle
94 C, 2 min / 98 C, 10 sec
68 C, 30 sec (25 cycles)
KME-101_example1-2.png M:1 kb DNA ladder
1:chromo9 1 kb
2:MSH6 1.8 kb
3:BRCA2 2.3 kb
4:WT-1 2.5 kb
5:FNCE 3 kb
6:RAD51D 4 kb
7:KRAS 5 kb
8:BRCA1 7 kb
9:DDB2 10 kb
MP: Multiplex PCR 1~9
 

Example 2.Amplification from bisulfite-treated DNA
The target DNAs (917–1,583 bp) were amplified using bisulfite-treated CpG-methylated Jurkat genomic DNA. All targets were successfully amplified using KOD -Multi & Epi-®.

KME-101_example2-1.png

M: 100 bp DNA ladder
1:TGFb 917 bp
2:BRCA2 1134 bp
3:APOE 1487 bp
4:TGFb 1583 bp
   

 
REFERENCES

  1. Takagi M, Nishioka M, Kakihara H, Kitabayashi M, Inoue H, Kawakami B, Oka M, and Imanaka T., Appl. Environ. Microbiol., 63: 4504–10 (1997)
  2. Hashimoto H, Nishioka M, Fujiwara S, Takagi M, Imanaka T, Inoue T and Kai Y, J. Mol. Biol., 306: 469–77 (2001)
  3. Mizuguchi H, Nakatsuji M, Fujiwara S, Takagi M and Imanaka T, J Biochem., 126:762-8 (1999)

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