GLDC (NM_000170) Human 3' UTR Clone

Specifications

Product Data
Product Name	GLDC (NM_000170) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	GCE; GCSP; HYGN1
ACCN	NM_000170
Insert Size	580 bp
Sequence Data	Insert Sequence (showhide) >SC207551 3’UTR clone of NM_000170 The sequence shown below is from the reference sequence of NM_000170. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTTTCTGAACAAAAGAGGGCGTCTTCTTAGTCCTCTGTCCCTAAGTTTAAAGGACTGATTTGATGCCTC TCCCCAGAGCATTTGATAAGCAAGAAAGATTTCATCTCCCACCCCAGCCTCAAGTAGGAGTTTTATATA CTGTGTATATCTCTGTAATCTCTGTCAAGGTAAATGTAAATACAGTAGCTGGAGGGAGTCGAAGCTGAT GGTTGGAAGACGGATTTGCTTTGGTATTCTGCTTCCACATGTGCCAGTTGCCTGGATTGGGAGCCATTT TGTGTTTTGCGTAGAAAGTTTTAGGAACTTTAACTTTTAATGTGGCAAGTTTGCAGATGTCATAGAGGC TATCCTGGAGACTTAATAGACATTTTTTTGTTCCAAAAGAGTCCATGTGGACTGTGCCATCTGTGGGAA ATCCCAGGGCAAATGTTTACATTTTGTATACCCTGAAGAACTCTTTTTCCTCTAATATGCCTAATCTGT AATCACATTTCTGAGTGTTCTCCTCTTTTTCTGTGTGAGGTTTTTTTTTTTTTAATCTGCATTTATTAG TATTCTAATAAAAGCATCTTGATCGGAA 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_000170.3
Synonyms	GCE; GCSP; HYGN1
Summary	Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).[provided by RefSeq, Jan 2010]
Locus ID	2731
MW	22.4

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