DNA Modifying EnzymesEukaryotic and prokaryotic cells possess multiple mechanisms to repair DNA and control damage to their genomes. These include base excision repair (BER) and nucleotide excision repair (NER) that excise and replace damaged nucleotide bases and helix-distorting lesions, respectively. Many of the enzymes involved in NER are also active in transcription-coupled repair (TCR) processes. In addition, mismatch repair (MMR) enzymes act to replace mismatched nucleotides and repair insertion/deletion loops. Furthermore, there are two types of double-stranded DNA break repair, homologous recombination (HR) and non-homologous end-joining (NHEJ).
Base excision repair proteins correct DNA lesions and ensure that mutations are not propagated. The process of base excision repair is achieved via specific and sequential enzyme activity. Damaged bases are first identified and removed by DNA glycosylases/AP lyases, which break beta-N glycosidic bonds to create an abasic (AP) DNA site. Depending on the initial events of base removal, repair proceeds through either the short patch (1 nucleotide) or long patch (2-10 nucleotides) repair pathways. This involves the AP site being recognized by endonuclease enzymes which nick the damaged DNA, and recruit DNA polymerases to fill the gap in the DNA. Base excision repair is completed by DNA ligase sealing the nick between the two strands.
Nucleotide excision is an additional DNA repair mechanism which removes nucleotides that have been damaged by chemicals or ultraviolet radiation. Nucleotide excision generates a short single-stranded DNA gap, which is subsequently used as a template by DNA polymerase. In addition to base and nucleotide excision repair molecules, mismatch repair (MMR) enzymes act to replace mismatched nucleotides and repair insertion/deletion loops. Genotoxic stress can introduce DNA double-strand breaks (DSBs), which are repaired by either homologous recombination or non-homologous end-joining. The Mre11/Rad50/Nbs1 (MRN) complex, along with members of the Rad51 family of proteins, are involved in double-strand break repair during homologous recombination. R&D Systems offers quality DNA enzyme products which include DNA glycosidases, endonucleases, polymerases, ligases, and more.
restriction enzymes
Restriction enzymes
Restriction Enzymes
DNA synthesis is catalyzed by enzymes called DNA polymerases. These enzymes are responsible for assembling new DNA strands by adding nucleotides to the growing chain during DNA replication.
DNA ligase
restriction enzymes
Restriction enzymes and DNA ligase are necessary to make recombinant DNA. Restriction enzymes are used to cut the DNA at specific sequences, while DNA ligase is used to join together pieces of DNA from different sources.
Restriction enzymes are used to cut DNA molecules in recombinant DNA research. These enzymes recognize specific DNA sequences and cleave the DNA at those sites, allowing scientists to splice DNA fragments from different sources together to create recombinant DNA molecules.
Screw Cap Tubes serve a broad range of laboratory needs, including collection, processing, centrifugation, long term storage and OEM packaging, shipping of restriction enzymes or other DNA/RNA modifying enzymes.
Enzymes that cut DNA at specific sites to form restriction fragments are called restriction endonucleases or restriction enzymes. These enzymes recognize specific DNA sequences and cleave the DNA at or near these sequences, generating DNA fragments with defined ends.
Yes, enzymes are commonly used in the process of cloning. Enzymes such as restriction enzymes are used to cut DNA at specific sites, while DNA ligase is used to join DNA fragments together. These enzymes are essential for generating recombinant DNA molecules during cloning.
Enzymes involved in DNA replication include DNA polymerase, helicase, primase, ligase, and topoisomerase. These enzymes work together to unwind the DNA helix, synthesize new DNA strands, and repair any mistakes that may occur during the process.
Restriction enzymes
Restriction Enzymes
DNA replication requires the aid of enzymes. Enzymes like DNA polymerase and helicase are crucial for unwinding the DNA double helix, synthesizing new DNA strands, and proofreading and repairing any errors that may occur during replication. Without these enzymes, DNA replication cannot proceed effectively and accurately.
DNA synthesis is catalyzed by enzymes called DNA polymerases. These enzymes are responsible for assembling new DNA strands by adding nucleotides to the growing chain during DNA replication.
DNA ligase