PEX12 (NM_000286) Human 3' UTR Clone

Specifications

Product Data
Product Name	PEX12 (NM_000286) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	PAF-3; PBD3A
ACCN	NM_000286
Insert Size	1017 bp
Sequence Data	Insert Sequence (showhide) >SC211689 3’UTR clone of NM_000286 The sequence shown below is from the reference sequence of NM_000286. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGATTAAACTCTACTCCCCTGAGAACTGAAAGGGAATCATGTCTTATCCTCACAACAAAAGTATTGCG CTGTAATGTCACAGAGCTGGTTTCAGCATGGTATTGAGTTGACACTTCTCAGCCTCAATTCATAACTAT ATGAACTTTAAATGATTATATGGATTTCTTTAAAAGGATATGCCCATTTGATCCTAACCTTTTAGCCTG CTCTCTAGAACCCTACTTACAGTTGACCAAGCTGCTTAAAGTAGAAGGATCAGGACTGGCAGGGGATAT GAGGGCCAGTGTAGAGATTAAACAGAATAATGAGTACACAAGTTTTTGCCTATCCCTTTCCTTAAAATA TAAGAAATAAAGGAGCTCTTACGAAAAACCCAGGTTAGACCGCATAAAAAATAAAGTGAACAGTGAGGT GGTAGCAAGACTTCTTTTTAGAAAAGAAAGCATTTACCTGCCTGTCTGTAAGGTGGAAATTTCATCAGT TTGCAAACGATAAGAAATGCAGACTTGCTCTTGATAGAAATGCTTAGAAACACTCTGGGGGGGAAAAAA GCTCCTTCCATATACTGTGAGACATTTGTTAAGTGACATCTATTGTTTATCAGCTTTTAAGGATAAAAA AGGTATTTTAAAAGTTGGATATTTAGGATATTTGAGGATATTCCTTTATGAGCTCTCCATATCCTTCTT GAGAAACTGGTTAAAAAAGGAATAGGGGTTGAGTGTTACAGAGAGTAGTCTGAAGATTCCTGTGTAAAA GCAAAGCTAACAAGCAATGAAGACATGAAGCAAAATACTAATCTAATTGTGTAAAGAAAGGATATTTTA ATAAGTTCTTTCTGCTTGCTGCTAAGAGTTTGCTAAAGTGTCATGAATTATTCTGGTTATTACTAAAGT TTCTATGAAACACTTAAGTAGATTTTAAGAATAAATGTTTCTGGAAAAGAACTATGTTATGATTTTGTA GAAATGTAAAGATTACTTGAGGTGTTTAAAATAAATTTTTCATTCAGACTA 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_000286.3
Synonyms	PAF-3; PBD3A
Summary	This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
Locus ID	5193
MW	39.3

*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.