Acyclic sesquiterpene synthase (TPS1), Recombinant Protein
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Acyclic sesquiterpene synthase (TPS1), Recombinant Protein

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Cat: RP10450
Size: 0.5 mg (E-Coli)/ 0.05 mg (Baculovirus)/ 0.5 mg (Yeast)/ 0.05 mg (Mammalian-Cell)/ 1 mg (E-Coli)/ 0.1 mg (Baculovirus)/ 1 mg (Yeast)/ 0.1 mg (Mammalian-Cell)
Species: Zea mays (Maize)
Datasheet:

Product Info

Full Product Name
Recombinant Zea mays Acyclic sesquiterpene synthase (TPS1), partial
Product Gene Name
TPS1 recombinant protein
Product Synonym Gene Name
TPS1
Purity
Greater or equal to 85% purity as determined by SDS-PAGE. (lot specific)
Sequence
FSSGGHALRF GSSLPCWRRT PTQRSTSSST TRPAAEVSSG KSKQHDQEAS EATIRQQLQL VDVLENMGIS RHFAAEIKCI LDRTYRSWLQ RHEEIMLDTM TCAMAFRILR LNGYNVSSDE LYHVVEASGL HNSLGGYLND TRTLLELHKA STVSISEDES ILDSIGSRSR TLLREQLESG GALRKPSLFK EVEHALDGPF
Sequence Positions
21-220;Partial
Format
Lyophilized or liquid (Format to be determined during the manufacturing process)
Host
E Coli or Yeast or Baculovirus or Mammalian Cell
Molecular Weight
67,350 Da
Storage
Store at -20℃. For long-term storage, store at -20℃ or -80℃. Store working aliquots at 4℃ for up to one week. Repeated freezing and thawing is not recommended.
Protein Family
Alpha-copaene synthase

NCBI/Uniprot Data

NCBI Accession #
NP_001105097.2
NCBI GI #
1143558483
NCBI GenBank Nucleotide #
NM_001111627.2
NCBI GeneID
541974
NCBI Official Full Name
acyclic sesquiterpene synthase
NCBI Official Symbol
tps1
NCBI Official Synonym Symbols
KS; eks1; GRMZM2G049538
NCBI Protein Information
acyclic sesquiterpene synthase
UniProt Gene Name
TPS1
UniProt Protein Name
Acyclic sesquiterpene synthase
UniProt Synonym Protein Names
(3R,6E)-nerolidol synthase (EC:4.2.3.49); Beta-farnesene synthase (EC:4.2.3.47); Farnesyl diphosphatase (EC:3.1.7.6); Terpene synthase 1
UniProt Primary Accession #
Q84ZW8
UniProt Secondary Accession #
Q9XEI5
UniProt Related Accession #
Q84ZW8
UniProt Comments
Involved in the formation of (E)-beta-farnesene and (3E)-4,8-dimethyl-1,3,7-nonatriene, key signal molecules in induced plant defense mediated by the attraction of enemies of herbivores. In the presence of geranyl diphosphate, catalyzes the formation of the acyclic monoterpens (3R)-linalool and geraniol. However, the in vitro rate of sesquiterpene formation is about four times higher than the rate of monoterpene formation.

For research use only, not for clinical use.