Our Products
Carrier RNA Poly(A) is a single-stranded RNA homopolymer. Carrier RNA is used for quantitative precipitation/purification of RNA and DNA Carrier RNA Poly(A) (polyadenylic acid) can be used to evaluate the binding of potential therapeutic agents to mRNA in drug development research. Carrier RNA that improves binding and recovery of low-concentrated viral RNA.
TRIzol Reagent (TransZol™) is a ready-to-use reagent for the isolation of total RNA from cells and tissues.Reagent is a complete, ready-to-use reagent for the isolation of high-quality total RNA or the simultaneous isolation of RNA, DNA, and protein from a variety of biological samples. This monophasic solution of phenol and guanidine isothiocyanate is designed to isolate separate fractions of RNA, DNA, and proteins from cell and tissue samples of human, animal, plant, yeast, or bacterial origin, within one hour.
Taq DNA Polymerase is a thermo stable DNA polymerase that exhibits a 5’→3’ polymerase activity and a 5’→3’exonuclease activity, with no 3’→5’exonuclease activity. Taq DNA Polymerase is purified from an Escherichia coli (E.coli) strain over expressing the gene of Thermus aquaticus DNA polymerase. Taq DNA polymerase is heat-stable and will synthesize DNA at elevated temperatures from single-stranded templates in the presence of a primer. Taq Polymerase is recommended for use in routine PCR reactions. We supplied Taq Polymerase with appropriate buffers. Usually 1-1.5 u of Taq DNA Polymerase is used in 50 µl of reaction mix. Higher Taq DNA Polymerase concentrations may cause synthesis of nonspecific products. However, if inhibitors are present in the reaction mix (e.g., if the template DNA used is not highly purified), higher amounts of Taq DNA polymerase (2-3 u) may be necessary to obtain a better yield of amplification products. No endonuclease, exonuclease, or bacterial DNA were detected in this kit.
Moloney Murine Leukemia Virus Reverse Transcriptase (H-) (M-MLV RT) is an RNA-dependent DNA polymerase that can be used in cDNA synthesis with long messenger RNA templates (>5kb). M-MLV Reverse Transcriptase (RT) is a product of the pol gene of M-MLV and consists of a single subunit with a molecular weight of 71kDa.Because RNase H activity can catalyze the degradation of RNA in the DNA/RNA hybrid strand, the template RNA may be degraded in the cDNA one-strand synthesis reaction. M-MLV (H-) Reverse Transcriptase is an M-MLV mutant with loss of RNase H activity obtained by site-directed mutagenesis. Compared with the common mutants obtained by deleting the RNase H domain, this product retains the complete protein structure, so it has the same polymerase activity as the wild type, and can be used for longer cDNA synthesis and full-length cDNA library Construction, etc. It also has strand displacement activity and can be used in experiments such as 5'RACE.
TRIzol Reagent (TransZol™) is a ready-to-use reagent for the isolation of total RNA from cells and tissues.Reagent is a complete, ready-to-use reagent for the isolation of high-quality total RNA or the simultaneous isolation of RNA, DNA, and protein from a variety of biological samples. This monophasic solution of phenol and guanidine isothiocyanate is designed to isolate separate fractions of RNA, DNA, and proteins from cell and tissue samples of human, animal, plant, yeast, or bacterial origin, within one hour.
Proteinase K is a Broad-Spectrum serine protease for general digestion of proteins in Biological samples. Enzyme is free from RNase and DNase activities. Proteinase K is stable in urea and SDS. Recommended working conc. for Proteinase K is 10-20 mg/ml in majority of applications.
TransPure™ (8 High Efficiency Silica Membrane Layer) RNA extraction columns are supplied with spin columns andcollection tubes. The columns provide fast and reliable extraction of highquality RNA from tissues, cells, plants and blood with a binding capacity of 50μg. Extracted RNA is ready for use in many downstream applications, includingNorthern Blot, real-time PCR, translation and primer extension.
Microcentrifuge tube is one of the basic requirements of a biological laboratory. Transiom makes 2.0 ml self stand microcentrifuge tubes. Microcentrifuge Tubes are made of plastic (polypropylene). Microcentrifuge tubes are suitable for both sterile and non-sterile conditions. Microcentrifuge tubes can easily be used for centrifugation in a microcentrifuge while balancing the rotor. Microcentrifuge Tubes are economical and very useful in DNA/RNA extraction, amplification, PCR, blotting experiments, gel electrophoresis etc or any molecular biology experiment.
RNase A, also known as ribonuclease A or pancreatic RNase, is an endonuclease that digests single-stranded RNA and specifically cleaves after pyrimidine nucleotides.Ribonuclease A (RNase A) is endonuclease-free and quality-controlled for use in plasmid purification procedures for digestion of RNA.RNAse A (bovine pancreas) supplied as white lyophilized powder which dissolves readily at concentration of 10-15 mg/ml in Nuclease free water to give a clear colourless solution.RNase A is often used in removing RNA contaminants from DNA or protein samples, and in RNA protection assays.
Transiom 100bp DNA ladder extended is precisely quantified and mixed during the production. 100bp DNA ladder extended is pre-mixed with loading dye and is ready to use. 100bp DNA ladder extended consists of purified DNA bands spanning from 100 base pair to 1500 base pairs or even higher, depending on the size of the ladder. They are used to identify the molecular weight of an unknown linear fragment of the DNA when loaded and run in agarose gel electrophoresis, along with the test samples. Transiom Ready to use 100bp DNA ladder extended are available for a wide application and analysis during electrophoresis. The concentration of each DNA bands also allows quantitative estimation of DNA fragments.
Transiom 1 kb DNA ladder is precisely quantified and mixed during the production. 1 kb DNA ladder is pre-mixed with loading dye and is ready to use. 1 kb DNA ladder consists of purified DNA bands spanning from 1, 000 base pair to 10, 000 base pairs or even higher, depending on the size of the ladder. They are used to identify the molecular weight of an unknown linear fragment of the DNA when loaded and run in agarose gel electrophoresis, along with the test samples. Transiom Ready to use 1 kb DNA ladder are available for a wide application and analysis during electrophoresis. The concentration of each DNA bands also allows quantitative estimation of DNA fragments.
Transiom 100bp DNA ladder is precisely quantified and mixed during the production. 100bp DNA ladder is pre-mixed with loading dye and is ready to use. 100bp DNA ladder consists of purified DNA bands spanning from 100 base pair to 1500 base pairs or even higher, depending on the size of the ladder. They are used to identify the molecular weight of an unknown linear fragment of the DNA when loaded and run in agarose gel electrophoresis, along with the test samples. Transiom Ready to use 100bp DNA ladder are available for a wide application and analysis during electrophoresis. The concentration of each DNA bands also allows quantitative estimation of DNA fragments.