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Flavonol synthase/flavanone 3-hydroxylase (FLS1), Recombinant Protein
Cat: RP00919
Size: 0.02 mg (E-Coli)/ 0.2 mg (E-Coli)/ 5x0.2 mg (E-Coli)
Species: Arabidopsis thaliana (Mouse-ear cress)
Datasheet:
Product Info
Full Product Name
Recombinant Arabidopsis thaliana Flavonol synthase/flavanone 3-hydroxylase (FLS1)
Product Synonym Names
Flavonol synthase/flavanone 3-hydroxylase; EC=1.14.11.23; EC=1.14.11.9; FLS 1
Product Gene Name
FLS1 recombinant protein
Product Synonym Gene Name
FLS1; At5g08640; MAH20.20
Purity
Greater or equal to 85% purity as determined by SDS-PAGE. (lot specific)
Sequence
MEVERVQDIS SSSLLTEAIP LEFIRSEKEQ PAITTFRGPT PAIPVVDLSD PDEESVRRAV VKASEEWGLF QVVNHGIPTE LIRRLQDVGR KFFELPSSEK ESVAKPEDSK DIEGYGTKLQ KDPEGKKAWV DHLFHRIWPP SCVNYRFWPK NPPEYREVNE EYAVHVKKLS ETLLGILSDG LGLKRDALKE GLGGEMAEYM MKINYYPPCP RPDLALGVPA HTDLSGITLL VPNEVPGLQV FKDDHWFDAE YIPSAVIVHI GDQILRLSNG RYKNVLHRTT VDKEKTRMSW PVFLEPPREK IVGPLPELTG DDNPPKFKPF AFKDYSYRKL NKLPLD
Sequence Positions
1-336aa; Full Length
Format
Lyophilized or liquid (Format to be determined during the manufacturing process)
Host
E Coli or Yeast or Baculovirus or Mammalian Cell
Molecular Weight
43.3 kDa
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.
NCBI/Uniprot Data
NCBI Accession #
NP_001190266.1
NCBI GI #
334187530
NCBI GenBank Nucleotide #
NM_001203337.1
NCBI GeneID
830765
NCBI Official Full Name
flavonol synthase 1
NCBI Official Symbol
FLS1
NCBI Official Synonym Symbols
ATFLS1; FLAVONOL SYNTHASE; flavonol synthase 1; FLS; FLS1; T2K12.5
NCBI Protein Information
flavonol synthase 1
UniProt Gene Name
FLS1
UniProt Synonym Gene Names
FLS
UniProt Protein Name
Flavonol synthase/flavanone 3-hydroxylase
UniProt Synonym Protein Names
FLS 1
UniProt Entry Name
FLS1_ARATH
UniProt Primary Accession #
Q96330
UniProt Secondary Accession #
O04730; O04731; O04732; O04830; O04831; O04832
UniProt Related Accession #
Q96330
UniProt Comments
Catalyzes the formation of flavonols from dihydroflavonols. It can act on dihydrokaempferol to produce kaempferol, on dihydroquercetin to produce quercitin and on dihydromyricetin to produce myricetin. In vitro catalyzes the oxidation of both enantiomers of naringenin to give both cis- and trans-dihydrokaempferol.
For research use only, not for clinical use.