PEX16 (NM_004813) Human 3' UTR Clone

Specifications

Product Data
Product Name	PEX16 (NM_004813) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	PBD8A; PBD8B
ACCN	NM_004813
Insert Size	621 bp
Sequence Data	Insert Sequence (showhide) >SC208004 3’UTR clone of NM_004813 The sequence shown below is from the reference sequence of NM_004813. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CAGAAAATCTACTTCTACAGTTGGGGCTGACAGACCTCCCGGAAGGAGGGTGTGGGGAGGGGTGGGGCA GGGAGCCCCTCTTCCCTAATAAAACTGACTCCGGCAGCGTCCCAGCGTGCGGCCTCTCCGTGCCTACCG GCCAGGCCCCACACACAGCCCTGGTCGCCACCAGCGTTCCTCCCAGGACACCCTTGACTGCGCTCTCCT GTGACGATGCCACTGCAGCCCGCACCTTGTCACTGCTGGGCCAAGAAGCCTTCACTAGGAGTGGGATCC AGGCTCCTCTCCCACAGAAAGCGGTGACTTCACCTCATGGAGCCCGGGAAGCTGCTCGCCTCGGCAGCC ATAGGAGCGAACACTGCTGCTCTCTCGCTGGCCCCTGGTGAGGACAGGAAGCCTGAACCCGGGTGATGG CTGAACGCTGCCCAGCGTGTCTTCTGGCTGGGGCCCTCCGTCTGCCCCTTCTCCGCAGGGCCCTGTGGC TCTGGCAGCCCCAGGCCATGGCGTTGCCAGCCTCCCTGTGACAGAGCCTGGTGAACAGTGAGCCTGGCT CCCACGCAAGTGGCACTTTAAGCCCTGCATCCTCGGTTGAGAGTAAAAGGCTTTTCTCCCTTAGAAAAA 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_004813.4
Synonyms	PBD8A; PBD8B
Summary	The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described. [provided by RefSeq, Jul 2008]
Locus ID	9409
MW	22.2

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