GCDH (NM_000159) Human 3' UTR Clone

Specifications

Product Data
Product Name	GCDH (NM_000159) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	ACAD5; GCD
ACCN	NM_000159
Insert Size	488 bp
Sequence Data	Insert Sequence (showhide) >SC206001 3’UTR clone of NM_000159 The sequence shown below is from the reference sequence of NM_000159. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GGAATCCAGGCGTTCACGGCCAGCAAGTGAGCCGCTCCATCAGGGGCCCGAAACTCTCAAGCCCCTTTC TGGAGAGATGCCTGGCTGGACCGTAGGAGCGCTGTGCTCTGAGCTTAGAAAGGGAGGTGGCGGATGGAG TGGGAAGTGAGAGACACTGATTTTTAAATATCAAAATTTCCCTTCTGAAGTCGTTCAGATGTGTTCCTT AAAAAGAAGATGGAATTCTCTGTAGAGCGTCTCAATCCACTTTTAACCATGGATGAGAGCAGACTCCAT TTACCCTGAAATAGCAGCTTCTCTTGAGAGGAGAGTGACATGGAAGCAACTCCGTCTGCTGCAGCTGAC CCCCTCACACTGAGTTCACAGTGCGCCCTCCCTCCCTCCCATCTGGGGGTAGTGCCTTATGCTGGGTGT TGGAGCAGAGTGAGGGAGAGGAAAATAAAGACCTGCACATCTGACCCCAAGGTGTCAGGCCGGTTTACT GGTAA ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites	SgfI-MluI
OTI Disclaimer	Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq	NM_000159.4
Synonyms	ACAD5; GCD
Summary	The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12. [provided by RefSeq, Mar 2013]
Locus ID	2639
MW	18.2

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.