PEX26 (NM_017929) Human 3' UTR Clone

Specifications

Product Data
Product Name	PEX26 (NM_017929) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	PBD7A; PBD7B; PEX26M1T; Pex26pM1T
ACCN	NM_017929
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC214281 3’UTR clone of NM_017929 The sequence shown below is from the reference sequence of NM_017929. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGCCTCTACCAGCTCCGCATCCGTGACTGAGGGTCCCTGCGCACCACAGCCTCTCTGCTCCTCACGTCC GTGGCCACAGAAGCAGAGCGACAGAGCGACACATCCACAGGCGCCCCTGGGGAAATGGGACCAGCCTAA TCTCGCGGAGTGCACTGTGTCTTGCTGCCTGGGTGCCCTCTCCTTTGCACCCTACTTCGGCTGGTCGCG GTAGATGATGTGGAAACAAAGCAGGACCAGCAGGCACAGCACCTCCAGAACAGTGCCCCGGATGACCAG AGGCCCCTTGAAAAGGAGGGGTTTGGGGACAGGGACTGTGTCCATGAAACATTCCATCTTCTTGGTGAA GGCAAGGGGTTGGTTCTTCAGGTCAGGATGTTAATGGAGCTGGAAGTTCAGAAAAAGCCTGGTGAAGTG ACCCTTGGCCTTTCACTTCTTGAGAAACATACTTCTTTGCTGGGCATGGTGACTCACGCCTGTAATCCC AGCACTTTGGAAGGGTGAGGTGGGTGGATCACTTGTGGCCAGGAGTTCAAAACCTGCCTGGCCAACATG GTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTAGATGTGGTGCACGCCTATAGTCCTAGCTAC TTGGGAGGCTGAGGCAGGAGAATCACTTGAGCCAGGGAGGCAAAAGTTGCAGTGAGCTGAGATTGTGCT ACCGCACTCTCTCAAAACAAACAAAAAAACATGCCCCACAGGACAGTACCTTAATTAGCTAGAGTAGAT CTGAGAGGGCCTCTTCTTGCCTGCACTGTGCTCCCCAGAGCTGATCTAATTCTGTATCAATAGGCTGTT CCCATGGTCTTGCCATGCGCTTGAAGCTGCAGGAGCCTTCTCACTGTTCAGGCTGGGGTGTGGTTTTCA GAACCACCGGGTTGACTACTGAAAACCAAGTGAGCCTTACAGCTCTTATCGCTGGGTAAAGTGATCTTG CCTGGTGCCTCTTGGTCTTCAGCTCAATTTTCCAGGTTGTCCTGGCCAAGTCTTGCTCTGTTACGCTCA GTGCCTCTGCCCACTCTTTCCCCGCCAGCCCTTCCCTCCCGCCCTGCAAACTTGTCCCTTGGCTGTTTC ACCAGGTTCTGCCTGTATCCTTGCCTCCTTGGTACACACCATTTCAGGTTCTTCCCTTTCTGTGTCCCA TTGTCCTAGTTATGTTCTGTTGTTTGTGTAATGCCCAAATTTTTCTGCTCGTGTGGCCTTGAAAAGTAG GCCAGCCTCAGAGGCTGCTGAGCTGAAAATGGAACTGAGTAATCAGGTGAGCTGGAAGGGATGTGGGGG GCGGGGCAGACGGGAGACATGGGTTTTGAAGGCAGTGAACAATAAAACCTTAGGGAGGTGGCACCGAGG CCTTAGCATTTGAGGAGCTGAAATGTTTCAGTGTTGTTTTCTCACCAGCCACAAGCATCTTATGAGTTT CTGTGCAAGGAAGCGTAGAGCACTGCTGTGCTGTCAGGATGAAGAAGGGCTTTCTGCAGGGGCTGGCCT TTCTCTACCCAGAGGCCAAGCAGGCTGCCCTGCACTGTGTCCTTGGTGTTGATGCCCAAAATAGAGAAG GTGCTTGCTAGCTTTTCCTTGGTACATTTTCGGGGGTTGCAAGGCAACAAGTTTTCTTTTGTTTTGTTT GTTTGTTTGTTTGTTTGTTTTTGAGATGGAGTCTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTC AGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGAC TACAGGTGCCCACCACCTCGCCTGGCTAATATTTTTGTATTTTTAGTAGAGTCTGGGTTTCACTGTGTT AGCCGGGATGGTCTCGATCTCCTGAACTTGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTAC AGGTGTGAGCCATCGCGCCCGGCCAACTTTTCTTTAGAAAAATGAGTAAAGTAGGTAAACTTCACAGG 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_017929.6
Synonyms	PBD7A; PBD7B; PEX26M1T; Pex26pM1T
Summary	This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010]
Locus ID	55670
MW	73.3

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