E2EPF, CT (Ubiquitin-conjugating Enzyme E2S, Ubiquitin-conjugating Enzyme E2-24kD, Ubiquitin-protein Ligase S, Ubiquitin Carrier Protein S, E2-EPF5, Ubiquitin-conjugating Enzyme E2-EPF5, UBE2S, E2EPF, OK/SW-cl.73)

  • Catalog number
    MBS631425
  • Price
    Please ask
  • Size
    0,2 mL
  • Other size
    please contact us to order other different size
  • Description
    A carrier can hold protected the subject it is supporting for the period needed by its application as stated by MyBioSource. Enzymes are cleaving the substrate. If the substrate is DNA they are called restriction enzymes. Activating enzymes will cut off the domain that is biological active to become functional.
  • Gene target
  • Gene symbol
    DLAT, DBT, UBE2S, SNORA62, DLST, NFE2, UBE2O, CST12P, SDR16C5, CDC34
  • Short name
    E2EPF, CT (Ubiquitin-conjugating Enzyme E2S, Ubiquitin-conjugating Enzyme E2-24kD, Ubiquitin-protein Ligase S, Ubiquitin Protein S, E2-EPF5, Ubiquitin-conjugating Enzyme E2-EPF5, UBE2S, E2EPF, OK/SW-cl 73)
  • Technique
    Enzyme, enzymes
  • Alternative name
    E2EPF, CT (Ubiquitin-conjugating Enzyme E2S, Ubiquitin-conjugating Enzyme E2-24kD, Ubiquitin-protein Ligase S, Ubiquitin Carrier Protein S, E2-EPF5, Ubiquitin-conjugating Enzyme E2-EPF5, UBE2S, E2EPF, OK/SW-cl.73)
  • Alternative technique
    enzymes
Gene info
Gene info
Gene info
Gene info
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    nuclear factor, erythroid 2
  • Synonyms gene name
    • nuclear factor (erythroid-derived 2), 45kD
    • nuclear factor (erythroid-derived 2), 45kDa
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1993-11-03
  • Entrez gene record
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • Basic leucine zipper proteins
  • VEGA ID
Gene info
Gene info
Gene info
Gene info
MeSH Data
  • Name
  • Concept
    Scope note: A DNA amplification technique based upon the ligation of OLIGONUCLEOTIDE PROBES. The probes are designed to exactly match two adjacent sequences of a specific target DNA. The chain reaction is repeated in three steps in the presence of excess probe: (1) heat denaturation of double-stranded DNA, (2) annealing of probes to target DNA, and (3) joining of the probes by thermostable DNA ligase. After the reaction is repeated for 20-30 cycles the production of ligated probe is measured.
  • Tree numbers
    • E05.393.620.311
  • Qualifiers
    ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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