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Fatty acid amide hydrolase (FAAH), Recombinant Protein
Cat: RP03278
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 Fatty acid amide hydrolase (FAAH)
Product Gene Name
FAAH recombinant protein
Purity
Greater or equal to 85% purity as determined by SDS-PAGE. (lot specific)
Sequence
MGKYQVMKRA SEVDLSTVKY KAETMKAPHL TGLSFKLFVN LLEAPLIGSL IVDYLKKDNG MTKIFRNTVI PEEPMFRPEF PSQEPEHDVV IVGEDESPID RLETALKCLP QYDPSRSLHA DPVSSFRYWK IRDYAYAYRS KLTTPLQVAK RIISIIEEFG YDKPPTPFLI RFDANEVIKQ AEASTRRFEQ GNPISVLDGI FVTIKDDIDC LPHPTNGGTT WLHEDRSVEK DSAVVSKLRS CGAILLGKAN MHELGMGTTG NNSNYGTTRN PHDPKRYTGG SSSGSAAIVA AGLCSAALGT DGGGSVRIPS ALCGITGLKT TYGRTDMTGS LCEGGTVEII GPLASSLEDA FLVYAAILGS SSADRYNLKP SPPCFPKLLS HNGSNAIGSL RLGKYTKWFN DVSSSDISDK CEDILKLLSN NHGCKVVEIV VPELEEMRAA HVISIGSPTL SSLTPYCEAG KNSKLSYDTR TSFAIFRSFS ASDYIAAQCL RRRLMEYHLN IFKDVDVIVT PTTGMTAPVI PPDALKNGET NIQVTTDLMR FVLAANLLGF PAISVPVGYD KEGLPIGLQI MGRPWAEATV LGLAAAVEEL APVTKKPAIF YDILNTN
Sequence Positions
1-607aa; full length protein
Format
Liquid containing glycerol
Host
Cell Free Expression
Molecular Weight
66,079 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
Fatty-acid amide hydrolase
NCBI/Uniprot Data
NCBI Accession #
NP_201249.2
NCBI GI #
186532737
NCBI GenBank Nucleotide #
NM_125840.3
NCBI GeneID
836565
NCBI Official Full Name
fatty acid amide hydrolase
NCBI Official Symbol
FAAH
NCBI Official Synonym Symbols
AtFAAH; FAAH; fatty acid amide hydrolase
NCBI Protein Information
fatty acid amide hydrolase
UniProt Gene Name
FAAH
UniProt Protein Name
Fatty acid amide hydrolase
UniProt Synonym Protein Names
N-acylethanolamine amidohydrolase
UniProt Entry Name
FAAH_ARATH
UniProt Primary Accession #
Q7XJJ7
UniProt Secondary Accession #
Q93ZI9; Q9FGF2; Q9LLC0
UniProt Related Accession #
Q7XJJ7
UniProt Comments
Degrades bioactive fatty acid amides to their corresponding acids, thereby serving to terminate the signaling functions of these molecules. Converts N-actylethanolamine (NAE) to ethanolamine. Can also use oleamide or 2-arachidonylglycerol as substrates, but not indole-3-acetamide, 1-naphtalene-acetamide, nicotinic acid amide or L-asparagine. Might be involved in abscisic acid signaling and plant defense through distinctly different mechanisms not involving the catalytic activity.
For research use only, not for clinical use.