Taq DNA polymerase is a thermostable enzyme isolated from E. coli which encodes Taq DNA polymerase gene. This enzyme contains 5’-3’ poly merase and 5’-3’ exonuclease activity .
• Amplification of DNA fragments up to 5 kb
• Labeling of PCR products with modified nucleotides (biotin-dUTP, fluorescein-dUTP)
• Cycle sequencing
• Generation of PCR product for TA cloning
DNA/RNA/Protein Isolation Kits
Description
This kit provides a rapid method for the high throughput isolation and purification of total RNA, DNA and proteins sequentially from a single sample of cultured animal cells, small tissue samples, blood, bacteria, or yeast.
Maximum Column Binding Capacity
50 μg for RNA 20 μg for DNA 200 μg for protein
Maximum Column Loading Volume
650 μL
Size of RNA Purified
All sizes, including small RNA (< 200 nt)
Size of DNA Purified
≥ 30 kb
Plasmid Genomics DNA Extraction Kit
Description
This miniprep Plasmid Kit was designed for plasmid DNA purification of cultured bacterial cells. For processing larger volumes.
Binding Capacity
50 µg
Culture Input
1-7 ml
Plasmid Size
1-15 kb
Typical Yield
up to 50 µg
Elution Volume
30-100 µl
PCR Purification/Clean Up Kits
Description
PCR Purification Kit is designed for the rapid purification of PCR Products > 100 bp. DNA of up to 10 kb is purified using a simple and fast bind-wash-elute procedure and an elution volume of 30–50 μl. An optional pH indicator allows easy determination of the optimal pH for DNA binding to the spin column.
PCR Purification procedure removes primers, nucleotides, enzymes, mineral oil, salts, and other impurities from samples and is compatible with restriction enzyme digestion, ligation into vectors and sequencing.
Binding Capacity
Up to 10 µg
Processing
Manual
Fragment size
100 bp – 10 kb
Elution Volume
>30 µl
One PCR Master Mix
Description
One-Step RT-PCR Mix is designed for performing highly sensitive and specific RT-PCR. The kit is based on a genetically engineered reverse transcriptase with enhanced thermal stability resulting in an increased specificity, high cDNA yield and an improved efficiency for highly structured and long cDNA fragments.The kits contain all reagents required for RT-PCR (except template and primer) in one kit combining simple handling with high flexibility. The premium quality polymerases, ultrapure dNTPs and the optimized complete reaction buffers ensure superior amplification results.RT-PCR is used to amplify double-stranded DNA from single-stranded RNA templates. In the RT step the reverse transcriptase synthesizes single-stranded DNA molecules (cDNA) complementary to the RNA template. In the first cycle of the PCR step synthesis, Taq DNA polymerase synthesizes DNA molecules complementary to the cDNA, thus generating a double-stranded DNA template. During subsequent rounds of cycling the DNA polymerase exponentially amplifies the double-stranded DNA template.In one-step RT-PCR all components of reverse transcription (RT) and PCR are mixed in one tube prior to starting the reaction and thus carried out sequentially without opening the tube. This offers tremendous convenience when applied to analysis of single targets from multiple samples of RNA and minimizes the risk of contaminations.
Biotin Labeling Kits
Description
Biotin Labeling Kit is designed
for simple and fast labeling of proteins
with biotin. The kit is ideally suited to label
antibodies, hormones or other proteins.
Labeling Reagent
750 µg
Dimethylsulfoxide (DMSO)
20 µl
Reaction Buffer
(0.1 M sodium phosphate, pH 8.0)
5 ml
Stop Reagent (1 M ethanolamine)
10 µl
Gel Filtration Slurry
5 ml
Agarose Avidin (1:1 slurry)
250 µl
Elisa Kits AND CONSUMABLES
Description
A wide range of ELISA Kits for Human Interleukin and Cytokine , Mouse Rat Porcine , QBlue Assay kits, Bio Assay Kits, Assay Kits, Mitochondria Isolation, Activity, GoldMag Nanoparticle, Total Protein Extraction Kit, Cloning Kits, DNA Extraction Kit Bacteria Identification Kit, QPCR & qRT PCR Products