UBC9, NT (SUMO-conjugating Enzyme UBC9, SUMO-protein Ligase, Ubiquitin-conjugating Enzyme E2 I, Ubiquitin-protein Ligase I, Ubiquitin Carrier Protein I, Ubiquitin Carrier Protein 9, p18, UBE2I, UBC9, UBCE9)[UBC9]

  • Catalog number
    MBS626003
  • Price
    Please ask
  • Size
    NA
  • Products_type
    Antibody
  • Reactivity
    Human
  • 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
    UBE2I, SUMO1
  • Short name
    UBC9, NT (SUMO-conjugating Enzyme UBC9, SUMO-protein Ligase, Ubiquitin-conjugating Enzyme E2 I, Ubiquitin-protein Ligase I, Ubiquitin Protein I, Ubiquitin Protein 9, p18, UBE2I, UBC9, UBCE9)[UBC9]
  • Technique
    Enzyme, enzymes
  • Host
    Rabbit
  • Alternative name
    UBC9, NT (SUMO-conjugating Enzyme UBC9, SUMO-protein Ligase, Ubiquitin-conjugating Enzyme E2 I, Ubiquitin-protein Ligase I, Ubiquitin Carrier Protein I, Ubiquitin Carrier Protein 9, p18, UBE2I, UBC9, UBCE9)[UBC9]
  • Alternative technique
    enzymes
Gene info
  • Identity
  • Gene
  • Long gene name
    ubiquitin conjugating enzyme E2 I
  • Synonyms gene name
    • ubiquitin-conjugating enzyme E2I (homologous to yeast UBC9)
    • ubiquitin-conjugating enzyme E2I (UBC9 homolog, yeast)
    • ubiquitin-conjugating enzyme E2I
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1995-07-11
  • Entrez gene record
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • Ubiquitin conjugating enzymes E2
  • VEGA ID
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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