Skip to Content
MilliporeSigma
All Photos(5)

Documents

2GFHSGKB

Roche

KAPA2G Fast HotStart Genotyping Mix

with dye

Synonym(s):

PCR, genotyping

Sign Into View Organizational & Contract Pricing


About This Item

UNSPSC Code:
41106300
NACRES:
NA.55

Quality Level

usage

sufficient for 100 reactions
sufficient for 500 reactions

shelf life

≤18 mo.

feature

Difficult Templates/Specialty Enzymes PCR
dNTPs included
hotstart

packaging

kit of 1.25 mL (100 x 25 μL rxn; KK5620)
kit of 6.25 mL (500 x 25 μL rxn; KK5621)

manufacturer/tradename

Roche

technique(s)

PCR: suitable
genotyping: suitable

input

crude DNA

storage temp.

−20°C

General description

KAPA2G Fast HotStart® Mouse Genotyping Kits include KAPA Express Extract, a novel thermostable protease and buffer system that allows for the extraction of PCR-ready DNA from mouse tissue in as little as 15 minutes, and KAPA2G Fast Genotyping Mix with dye, containing a DNA polymerase engineered via directed evolution for high processivity and extreme speed. The combination of KAPA Express Extract and KAPA2G Fast Genotyping Mix allows for the reliable extraction and amplification of DNA fragments from mouse tissue in as little as 1 hour, as compared to ≥1 day with conventional protocols. KAPA2G Fast Genotyping Mix (2X) is a ready-to-use master mix containing all components for fast PCR with stabilizers, two inert dyes except primers and template.

Application

KAPA2G Fast HotStart® Genotyping Mix has been used in:
  • Genomic DNA extraction and in the preparation of master mix for PCR
  • Extraction and amplification from mouse tail, ear, and toe tissue
  • Extraction and amplification of DNA from other animal tissues

Biochem/physiol Actions

KAPA2G Fast Genotyping Mix generated DNA fragments are 3′-dA-tailed and may be cloned into TA cloning vectors, or used for routine downstream analyses or applications, including restriction enzyme digestion, cloning and sequencing. Like wild-type Taq, KAPA2G Fast has 5′→3′ polymerase and 5′→3′ exonuclease activities, but no 3′→5′ exonuclease (proofreading) activity. The fidelity of KAPA2G Fast is similar to that of wild-type Taq; it has an error rate of approximately 1 error per 1.7 x 105 nucleotides incorporated. Unlike existing protocols that rely on Proteinase K digestion, extractions using KAPA Express Extract are conveniently performed in a single tube, without the need for hazardous chemicals, or multiple wash steps.

Features and Benefits

Increased throughput, turnaround time and reliability:
  • PCR-ready DNA generated in as little as 15 minutes
  • Minimal handling, thereby reducing the risk of sample loss or contamination
  • Sufficient template for multiple assays; easily scaled to handle samples in a 96-well format
  • Fast and reliable amplification of DNA fragments across a wide range of amplicon lengths and GC contents

Outperforms crude extraction methods and commercial kits:
  • Increased turnaround times
  • Increased specificity
  • Decreased cost

Quick Notes:
  • Extract PCR-ready DNA from mouse tail, ear, or toe tissue in 15 minutes
  • Dilute DNA extract 10-fold prior to PCR in 10 mM Tris-HCl (pH 8.0-8.5), and use 1 μL of DNA per 25 μL reaction.
  • Extracts are stable at -20°C for >6 months.
  • KAPA2G Fast (HotStart) Genotyping Mix contains the engineered KAPA2G Fast DNA Polymerase for fast PCR, along with buffer, MgCl2 (1.5 mM at 1X), and dNTPs (0.2 mM each at 1X).
  • Loading dye for electrophoresis is included in the KAPA2G Fast Genotyping Mix, which allows direct loading of PCR products onto agarose gels for analysis.
  • Use 15 sec annealing time, with 15 sec extension time for amplicons <1 kb, or 15-30 sec/kb extension for longer amplicons.

Packaging

  • 2X KAPA2G Fast Standard or HotStart Genotyping Mix with dye
Ships on Dry Ice in some cases however, shipping conditions may vary in certain regions.

Quality

All components contained with KAPA2G Fast HotStart Mouse Genotyping Kits are subjected to stringent quality control tests, are free of contaminating exo- and endonuclease activities and meet strict requirements with respect to DNA contamination.

Preparation Note

Always ensure that the product has been fully thawed and mixed before use. Reagents may be stored at 4°C for short-term use (up to 1 month). Return to -20°C for long-term storage. Provided that all components have been handled carefully and not contaminated, the kit is not expected to be compromised if left (unintentionally) at room temperature for a short period of time (up to 3 days).

Other Notes

For Research Use Only. Not for use in diagnostic procedures.

Legal Information

HOTSTART is a registered trademark of Molecular BioProducts, Inc.

Pictograms

Health hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

STOT SE 2

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Neuronal glutamate transporters control dopaminergic signaling and compulsive behaviors.
Bellini S, et al.
The Journal of Neuroscience, 38(4), 937-961 (2018)
Loss of TLR4 in mouse Muller cells inhibits both MyD88-dependent and?independent signaling.
Liu L and Jena J S
PLoS ONE, 12(12), e0190253-e0190253 (2017)
Matteo Rossi Sebastiano et al.
Science advances, 6(44) (2020-11-01)
Pancreatic ductal adenocarcinoma (PDAC) is characterized by marked fibrosis and low immunogenicity, features that are linked to treatment resistance and poor clinical outcomes. Therefore, understanding how PDAC regulates the desmoplastic and immune stromal components is of great clinical importance. We
Yves Laumonnier et al.
Current protocols in immunology, 130(1), e100-e100 (2020-07-28)
The anaphylatoxins (AT) C3a and C5a are effector molecules of C3 and C5 exerting multiple biologic functions through binding and activation of their cognate G protein-coupled receptors. C3a interacts with the C3a receptor (C3aR), whereas C5a and its primary degradation
Maria Saliakoura et al.
Oncogene, 39(14), 2948-2960 (2020-02-09)
Enhanced prostaglandin production promotes the development and progression of cancer. Prostaglandins are generated from arachidonic acid (AA) by the action of cyclooxygenase (COX) isoenzymes. However, how cancer cells are able to maintain an elevated supply of AA for prostaglandin production

Articles

An overview of directed evolution and the methods for generating proteins with optimized or entirely new functions.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service