PEX5 (NM_000319) Human Untagged Clone

CAT#: SC119969

PEX5 (untagged)-Human peroxisomal biogenesis factor 5 (PEX5), transcript variant 2


  "NM_000319" in other vectors (4)

Reconstitution Protocol

USD 310.00

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PEX5
Synonyms PBD2A; PBD2B; PTS1-BP; PTS1R; PXR1; RCDP5
Vector pCMV6-Entry
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>NCBI ORF sequence for NM_000319, the custom clone sequence may differ by one or more nucleotides


ATGGCAATGCGGGAGCTGGTGGAGGCCGAATGCGGGGGTGCCAACCCGCTCATGAAGCTCGCCGGGCACT
TCACCCAGGACAAGGCCCTTCGGCAGGAGGGATTGAGGCCTGGCCCCTGGCCCCCCGGAGCCCCGGCCTC
TGAGGCAGCCTCCAAGCCTTTGGGAGTAGCTTCTGAAGATGAGTTGGTGGCTGAATTCCTGCAGGACCAG
AATGCACCCCTTGTGTCCCGTGCCCCTCAGACCTTCAAGATGGATGACCTCCTGGCTGAGATGCAGCAGA
TTGAGCAGTCAAACTTCCGCCAGGCTCCCCAGAGAGCCCCTGGTGTGGCAGACTTGGCCTTGTCTGAGAA
CTGGGCCCAGGAGTTTCTTGCAGCTGGAGATGCTGTGGATGTAACTCAGGATTATAATGAGACTGACTGG
TCCCAAGAATTCATCTCTGAAGTTACAGACCCCTTGTCTGTGTCCCCTGCCCGCTGGGCTGAGGAATATT
TGGAGCAATCAGAGGAGAAGCTGTGGCTGGGAGAACCTGAGGGAACAGCCACCGATCGCTGGTATGATGA
ATATCATCCTGAGGAGGATCTGCAGCACACGGCCAGTGACTTTGTGGCCAAAGTGGATGACCCCAAATTG
GCTAATTCTGAGTTCCTGAAATTCGTGCGGCAGATTGGCGAAGGGCAGGTGTCCCTGGAGTCCGGTGCAG
GGTCGGGCCGAGCTCAGGCAGAACAGTGGGCAGCAGAGTTTATACAGCAGCAGGGTACATCAGATGCCTG
GGTTGACCAGTTCACAAGACCAGTAAACACATCTGCCCTTGATATGGAGTTTGAACGAGCCAAGTCAGCT
ATAGAGTTGCAGGCAGAGTTGGAGGAGATGGCAAAACGGGATGCTGAGGCCCACCCCTGGCTTTCTGACT
ATGATGACCTTACGTCAGCTACCTATGATAAGGGGTACCAGTTTGAGGAGGAGAACCCCTTGCGTGATCA
CCCTCAGCCTTTTGAAGAAGGGCTGCGGCGCCTTCAGGAGGGGGACCTGCCAAATGCTGTGCTGCTTTTT
GAGGCAGCTGTGCAGCAGGATCCTAAGCACATGGAAGCTTGGCAGTATCTGGGTACCACCCAGGCAGAGA
ATGAACAAGAACTATTAGCCATCAGTGCATTGCGGAGGTGTCTGGAGCTAAAGCCAGATAACCAGACAGC
ACTGATGGCGCTGGCTGTGAGCTTCACCAACGAGTCCCTGCAGCGACAGGCCTGTGAAACCCTACGAGAC
TGGCTGCGGTACACACCAGCCTATGCCCATCTGGTGACACCTGCTGAAGAAGGGGCTGGTGGGGCAGGAC
TGGGCCCCAGCAAGCGTATCCTGGGATCTCTCTTGTCTGACTCCCTGTTTCTTGAAGTGAAAGAGCTCTT
CCTGGCAGCTGTGCGGCTGGACCCTACCTCCATTGACCCTGATGTGCAGTGTGGCTTGGGAGTCCTTTTC
AACCTGAGTGGGGAGTATGACAAGGCCGTGGACTGCTTCACAGCTGCCCTCAGCGTTCGTCCCAATGACT
ATTTGCTGTGGAATAAGCTAGGCGCCACCCTGGCCAATGGAAACCAGAGTGAAGAAGCAGTAGCTGCGTA
CCGCCGGGCCCTCGAGCTCCAGCCTGGCTATATCCGGTCCCGCTATAACCTGGGCATCAGCTGCATCAAC
CTCGGGGCTCACCGGGAGGCTGTGGAGCACTTTCTGGAGGCCCTGAACATGCAGAGGAAAAGCCGGGGCC
CCCGGGGTGAAGGAGGTGCCATGTCGGAGAACATCTGGAGCACCCTGCGTTTGGCATTGTCTATGTTAGG
CCAGAGCGATGCCTATGGGGCAGCCGACGCGCGGGATCTGTCCACCCTCCTAACTATGTTTGGCCTGCCC
CAGTGA


>OriGene 5' read for NM_000319 unedited
GCATTTTGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACCAGCCGGGGTCCAG
GCCCCTTTGTGGAGGCAGCTGCTGGCCCCCAGCCCATGGGACCGTAGTCGCGGAGGCCTC
TGCAGAGGCGCAGGCTGGAAGCGGTGGCCTTTGAGGGGGGCGGCAGGAGAGAGTACCGAC
CTCCCTCGAACTCCTGGCAGAGAGAGCTGGCGGTCACCATGGCAATGCGGGAGCTGGTGG
AGGCCGAATGCGGGGGTGCCAACCCGCTCATGAAGCTCGCCGGGCACTTCACCCAGGACA
AGGCCCTTCGGCAGGAGGGATTGAGGCCTGGCCCCTGGCCCCCCGGAGCCCCGGCCTCTG
AGGCAGCCTCCAAGCCTTTGGGAGTAGCTTCTGAAGATGAGTTGGTGGCTGAATTCCTGC
AGGACCAGAATGCACCCCTTGTGTCCCGTGCCCCTCAGACCTTCAAGATGGATGACCTCC
TGGCTGAGATGCAGCAGATTGAGCAGTCAAACTTCCGCCAGGCTCCCCAGAGAGCCCCTG
GTGTGGCAGACTTGGCCTTGTCTGAGAACTGGGCCCAGGAGTTTCTTGCAGCTGGAGATG
CTGTGGATGTAACTCAGGATTATAATGAGACTGACTGGTCCCAAGAATTCATCTCTGAAG
TTACAGACCCCTTGTCTGTGTCCCCTGCCCGCTGGGCTGAGGAATATTTGGAGCAATCAG
AGGAGAAGCTGTGGCTGGGAGAACCTGAGGGAACAGCCACCGATCGCTGGTATGATGAAT
ATCATCCTGAGGAGGATCTGCAGCACACGGGCCAGTGACTTTGTGGCCAAAGTGGATGAC
CCCCAATGGGCTATTCTNGAGGACATCANATGCCTGGGTGACCGNTCACAAGACGTAACA
CTCTGCCTTGATATGGAGTTGACGAGCAGTCACTTAGATCTGAGTCGATTCTGGGACAN
>OriGene 3' read for NM_000319 unedited
NCCCTCGGTGNACCCGGCCGCAATCNANGATCGAGNTTTTTTTTTTTTTTTTTTTACGTT
TTTTTTTTTTTTTTTTTTTTTTTTTCCCACATAAGTTCCTTTTATTTTTCGAACAAAATT
TTAACAGTTTTATTTTTAAATCTTTAACCCTTTTTCTTACAAAAAAAAATAATTTTCAGG
ATGGAATCCTGGGCCCATGGAAGTTAAAAAAAAAAATTTTTTTGATCTTTACCTCCTAAA
AACAAGGCAAGAGGCTTACCAGCAATTTCTGGGGGTTAGGGTTTCCCCCCATGCGGGGGA
CACTGGAAAAAATCCCAAGCGTGCCCCTCATTTTCCTTCAACCCAAAGGGGGGAAGGGGA
TTTTCACATGCCTTCCCTTAAAAACCTTCCCCAAAACACTCACTAAGGGTTTAGGGCACC
CCTGACCCTTTCCGCCTACAACTTGGCACCGATGCGCTCTCCTCCCACCCCTTCTCTCTT
CCCTGCTGCCTTATCACACGTTTTCCCCTTTCTTCTCTCCAGCTCTCCCGCATTCCCCCC
CCTCTCCTCTACTCTCCGCCCCCCTCCCTCCGCTCCTTCCCCCCCCCCCGTCCTTACTCA
TCGCTCTTGCCCCCCCATTCCGCTCCACCTGACCCCCGCATCTCTCTCTTAGCCACCTCC
CCTCCTAACCCCTCCATCCCCCGACCCTATCCCCGGTCCTCTCTACCTTGCCATTCTCCC
CCCTTCCTCACGTCCTCCTCCCTCACGTCCTCCAAACCCTCCCTTCCCCCCACCGTACTC
ATTTATTCCGGTTGTATATATTCCCACCCTCATCCCCGCACTCAACCATATCCACCTAAA
CATCCTCTCTTCCTCCTCCCCCCCTCTCTCATATCACATCCCTCTCCCTCCCACCTTTTG
TTATATGTCATCTCTCTCCTGACACCCACTATCCTTTTAATTCGTAGTTCCCTTCTCCCT
CCCCTCTCTATATCTCCTTGT
Restriction Sites NotI-NotI     
ACCN NM_000319
Insert Size 3270 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_000319.3, NP_000310.2
RefSeq Size 3215 bp
RefSeq ORF 1896 bp
Locus ID 5830
Cytogenetics 12p13.31
Domains TPR
Protein Families Druggable Genome
Gene Summary 'The product of this gene binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import. 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 neonatal adrenoleukodystrophy (NALD), a cause of Zellweger syndrome (ZWS) as well as may be a cause of infantile Refsum disease (IRD). Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]'
Transcript Variant: This variant (2) differs in the 5' UTR, initiates translation from a downstream start codon, and uses an alternate splice site in the central coding region, compared to variant 6. The encoded isoform (b) has a shorter N-terminus compared to isoform e.

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