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]
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Catalog numberMBS626003
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PricePlease ask
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SizeNA
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Products_typeAntibody
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ReactivityHuman
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DescriptionA 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.
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Gene target
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Gene symbolUBE2I, SUMO1
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Short nameUBC9, 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]
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TechniqueEnzyme, enzymes
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HostRabbit
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Alternative nameUBC9, 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]
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Alternative techniqueenzymes
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Gene info
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Identity
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Gene
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Long gene nameubiquitin conjugating enzyme E2 I
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Synonyms gene name
- ubiquitin-conjugating enzyme E2I (homologous to yeast UBC9)
- ubiquitin-conjugating enzyme E2I (UBC9 homolog, yeast)
- ubiquitin-conjugating enzyme E2I
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Synonyms
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GenBank acession
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Locus
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Discovery year1995-07-11
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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Classification
- Ubiquitin conjugating enzymes E2
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VEGA ID
Gene info
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Identity
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Gene
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Long gene namesmall ubiquitin like modifier 1
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Synonyms gene
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Synonyms gene name
- ubiquitin-like 1 (sentrin)
- SMT3 suppressor of mif two 3 homolog 1 (yeast)
- SMT3 suppressor of mif two 3 homolog 1 (S. cerevisiae)
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Synonyms
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GenBank acession
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Locus
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Discovery year1996-06-04
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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VEGA ID
MeSH Data
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Name
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ConceptScope 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.
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Tree numbers
- E05.393.620.311
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Qualifiersethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data