PCCB (NM_000532) Human 3' UTR Clone

Specifications

Product Data
Product Name	PCCB (NM_000532) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_000532
Insert Size	173 bp
Sequence Data	Insert Sequence (showhide) >SC201539 3’UTR clone of NM_000532 The sequence shown below is from the reference sequence of NM_000532. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGGAGAAAACATGCAAATATTCCATTGTAAACAAATCAAAGGAAAAGAAACCAAGAACTGAATTACTGT CTGCCCATTCACATCCCATTCCTGCCTTTTGCAATCATGAAACCTGGGAATCCAAATAGTTGGATAACT TAGAATAACTAAGTTTATTAAATTCTAGAAAGATC 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_000532.5
Summary	The protein encoded by this gene is a subunit of the propionyl-CoA carboxylase (PCC) enzyme, which is involved in the catabolism of propionyl-CoA. PCC is a mitochondrial enzyme that probably acts as a dodecamer of six alpha subunits and six beta subunits. This gene encodes the beta subunit of PCC. Defects in this gene are a cause of propionic acidemia type II (PA-2). Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010]
Locus ID	5096
MW	6.8

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