Beta-carotene 3-hydroxylase 2 (BETA-OHASE 2), Recombinant Protein
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Beta-carotene 3-hydroxylase 2 (BETA-OHASE 2), Recombinant Protein

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Cat: RP00454
Size: 0.02 mg/ 0.1 mg/ 5x0.1 mg
Species: Arabidopsis thaliana (Mouse-ear cress)
Datasheet:

Product Info

Full Product Name
Recombinant Arabidopsis thaliana Beta-carotene 3-hydroxylase 2, chloroplastic (BETA-OHASE 2)
Product Gene Name
BETA-OHASE 2 recombinant protein
Product Synonym Gene Name
B2; CHY2
Purity
Greater or equal to 85% purity as determined by SDS-PAGE. (lot specific)
Sequence
EERKQSSPMD DDNKPESTTS SSEILMTSRL LKKAEKKKSE RFTYLIAAVM SSFGITSMAI MAVYYRFSWQ MKGGEVSVLE MFGTFALSVG AAVGMEFWAR WAHRALWHDS LWNMHESHHK PREGAFELND VFAITNAVPA IGLLYYGFLN KGLVPGLCFG AGLGITMFGM AYMFVHDGLV HKRFPVGPIA NVPYLRKVAA AHQLHHTDKF KGVPYGLFLG PKEVEEVGGK EELEKEISRR IKLYNKGSST S
Sequence Positions
53-303aa; full length protein
Format
Liquid containing glycerol
Host
Cell Free Expression
Molecular Weight
25,928 Da
Storage
Store at -20℃, for extended storage, conserve at -20℃ or -80℃.Repeated freezing and thawing is not recommended. Store working aliquots at 4℃ for up to one week.
Protein Family
Beta-carotene 3-hydroxylase

NCBI/Uniprot Data

NCBI Accession #
NP_001119420.1
NCBI GI #
186531513
NCBI GenBank Nucleotide #
NM_001125948.1
NCBI GeneID
835334
NCBI Official Full Name
beta-carotene hydroxylase 2
NCBI Official Symbol
BETA-OHASE 2
NCBI Official Synonym Symbols
B2; BCH2; BETA CAROTENOID HYDROXYLASE 2; beta-carotene hydroxylase 2; BETA-OHASE 2; CHY2; F6N7.5; F6N7_5; FERREDOXIN-DEPENDENT DIIRON OXYGENASE
NCBI Protein Information
beta-carotene hydroxylase 2
UniProt Gene Name
BETA-OHASE 2
UniProt Synonym Gene Names
B2; CHY2; AtB2
UniProt Protein Name
Beta-carotene 3-hydroxylase 2, chloroplastic
UniProt Entry Name
BCH2_ARATH
UniProt Primary Accession #
Q9LTG0
UniProt Secondary Accession #
B3H4E9
UniProt Related Accession #
Q9LTG0
UniProt Comments
Nonheme diiron monooxygenase involved in the biosynthesis of xanthophylls. Specific for beta-ring hydroxylations of beta-carotene. Has also a low activity toward the beta- and epsilon-rings of alpha-carotene. No activity with acyclic carotenoids such as lycopene and neurosporene. Uses ferredoxin as an electron donor (Probable).

For research use only, not for clinical use.