Tool Enzyme

Bsu DNA polymerase, Large fragment is a polymerase derived from Bacillus subtilis. Bsu DNA polymerase, Large fragment is a DNA isothermal amplification polymerase with chain replacement activity, which used in RPA recombinase polymerase amplification technology.

Recombinant Proteinase K is a serine protease that cleaves the carboxy-terminated peptide bonds of aliphatic and aromatic amino acids. Recombinant Proteinase K can be used to digest proteins and remove contamination from nucleic acid preparations.

Acetolactate synthase (Crude Enzyme) (EC 2.2.1.6) is a transferase that can convert 2 pyruvate and H⁺ into (2S)-2-acetolactate and CO₂.

AceTaq DNA polymerase is a transferase that can convert DNA(n) and a 2'-deoxyribonucleoside 5'-triphosphate into DNA(n+1) and diphosphate.

A blend of enzymes for coffee is a blend of enzymes that can catalyze be used in coffee processing.

5-Phytase (EC 3.1.3.72) is a hydrolase that can convert 1D-myo-inositol hexakisphosphate and H₂O into 1D-myo-inositol 1,2,3,4,6-pentakisphosphate and phosphate.

α-Factor-transporting ATPase (EC 7.4.2.7) is a plasma membrane ATP-binding cassette (ABC) transporter that actively exports the farnesylated lipopeptide mating pheromone a-factor from the cytosol of MATa haploid cells.

β-Glucan-transporting ATPase (EC 7.5.2.3) can be used to investigate the application of β-glucan-transporting ATPase in carbohydrate transport research.

Terminal Transferase, Calf (EC 2.7.7.31) is a template independent polymerase that catalyzes the addition of deoxynucleotides to the 3' hydroxyl terminus of DNA molecules. Protruding, recessed or blunt-ended double or single-stranded DNA molecules serve as a substrate for Terminal Transferase. Terminal Transferase does not have 5' or 3' exonuclease activity. The addition of Co²⁺ in the reacton makes tailing more efficient.

Enterokinase, Porcine (EC 3.4.21.9), is an enzyme produced by duodenal cells and participates in the digestive process in humans and animals. Enterokinase converts trypsinogen (an enzyme precursor) into its active form, trypsin, thereby activating pancreatic digestive enzymes. Deficiency of enterokinase can lead to intestinal digestive dysfunction.

Polymyxin Acylase, Pseudomonas sp. deacylates polymyxin group antibiotics and long-chain fatty acyl groups of proteins.

Human alkyl adenine DNA glycosylase is a monomeric DNA glycosylase that corrects a broad range of alkylated and deaminated nucleobases to maintain genomic integrity.

DNA polymerase, NeoApollonia Thermophilus is a thermostable DNA polymerase from Streptococcus thermophilus that can be used in PCR reactions. DNA polymerase, NeoApollonia Thermophilus has 3’→5’ and 5’→3’ exonuclease activities.

E. coli DNA ligase is a NAD⁺-dependent DNA ligase that catalyzes the formation of a phosphodiester bond between the complementary 3′-OH and 5′-P ends of dsDNA.

T4 lysozyme is derived from a recombinant E.coli strain and can lyse bacterial cell walls. T4 lysozyme acts on the peptidoglycan of bacterial cell walls and hydrolyzes the β-1,4 bond between N-acetylmuramic acid and N-acetylglucosamine.

DNA Recombinase is a simple and efficient multi-segment recombinase mixture that can assemble single or multiple DNA fragments into a complete plasmid by recognizing the DNA insert and the homology arms (17bp-50bp) at the ends of the linearized vector, regardless of the length of the fragment or the end compatibility.

T4 Phage β-glucosyltransferase is a DNA-modifying enzyme encoded by bacteriophage T4. T4 Phage β-glucosyltransferase transfers glucose from uridine diphosphoglucose to 5-hydroxymethyl cytosine bases of phage T4 DNA.

Phosphopentomutase is an oxidase. Enzymes have high catalytic efficiency, high specificity, and mild operating conditions. It can be applied in industries such as pharmaceuticals, industrial production, food manufacturing, and aquaculture.

Cyclomaltodextrinase is a hydrolase. Enzymes have high catalytic efficiency, high specificity, and mild operating conditions. It can be applied in industries such as pharmaceuticals, industrial production, food manufacturing, and aquaculture.

Thermostable T7 RNA Polymerase is a thermostable version of T7 RNA Polymerase (HY-E70090). Compared with T7 RNA Polymerase, it has high temperature resistance and stable activity. T7 RNA polymerase is a polymerase expressed by Escherichia coli from the RNA polymerase gene of T7 bacteriophage. T7 RNA polymerase is highly specific and involved in in vitro transcription (IVT) of mRNA. In the presence of Mg²⁺, T7 RNA polymerase only uses the single-stranded or double-stranded DNA containing the T7 promoter sequence as a template, and uses NTP as a substrate to synthesize RNA complementary to the single-stranded DNA downstream of the promoter.