PEX3 (NM_003630) Human 3' UTR Clone

CAT#: SC214325

3' UTR clone of peroxisomal biogenesis factor 3 (PEX3) for miRNA target validation



Need custom modification / cloning service?
Get a free quote

CNY 4845.00


货期*
3周

规格
    • 10 ug

Product images

推荐一起购买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1280.00

Specifications

Product Data
Product Name PEX3 (NM_003630) Human 3' UTR Clone
Vector pMirTarget
Synonyms PBD10A; PBD10B; TRG18
ACCN NM_003630
Insert Size 1420 bp
Sequence Data
>SC214325 3’UTR clone of NM_003630
The sequence shown below is from the reference sequence of NM_003630. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
TTTAGTACCCCTCAGCAACTGGAGAAATGATTTTTCCTTCAAGAAAAACTACAGTGGGATTCATTTACT
TTTTAAAATACACTGGGTAAATCACCTATACTTAGAGTAACAGTTTGTTATCAAAATGCCTGATAAAAT
ATATTCTTAATAAAAGTCTTCATTTCATAATGAAATCAATTTATTTGGCATCTTAATATATTTTTTTAG
ATTCATCAACAGACCAGTTTTTGTGGGCATATATATATACACGTGCAAATATCAGAATTGTTAATAATT
TGTTACACATGGACATTTGTTCCAAACTGACTAAAAATCAATATAGATATTTTATATACATATATATAT
ATAAAAATACAAAATTCAGTGTACTTTACCATATTAATACTGAGGAAAAATCTGTTGGAGACATAGGTC
TAGGATGTGTGAAGTTTGGAAAAATATGCTATTTAATTATAATGTTCCCTAGACTGCTGTAAACAGAAG
TGAATCAGACTTTTCTCCAGCTACCTTTCAAAATAATAAATTATTTGTCTCAAATATACCTTGATGGAG
GACTTTTTTATTCTTATGGAAATAGTGAATTCCAACAACTATGATGAACTATGTTCTTTGCTATTTCTT
CACTATATTTTTTAAGGTTTTATTAAAAAGCCTTAGAAAGTTACATATTGGTTTAGAGGCTAAAATTGT
GTTGATGCTGTTTACTCACCTAATTACATAGTTTTAATCATTTGTACATAATTTTAAAAACTTACTTTG
TATTGATTTTGAATACAGTGAAAATCTTATTGCAATAAACTATTTTAGTAAAATATTATTTTGTTGAGT
TAATATTTTTCAGCTATTAATTTACTTATCCCATAGCATTTTTGTTATTATTTCGGAAGAGAGAGCATG
CTAGTTTAAGTTTCATTTTAATTGGTCGTGTACTTGGTGCTTTTTTGTTGTTGTTAACTTGTTCATTTA
GTAAAAAGCAAATAGCTTTACTTTCTGAAAAAGAAATAATTCATTATCTCTAGTAATACATCTGTAATT
CTTCATTTAGAAGGGTAATTAGGGCAAAAGTAAATAAATCATTATATATCATTAGTATGTTGACATATA
TTTTCAGTAACATTGTTTTATGTTCCTCCAGCGTAACATGTAGCTGAACAGTAGAAGGTAGAAAATAAA
TTATGACATCTCTTCTAAGGCCTGGCTAGGCCTGAAGCTCACTGCCAGGGAGTTTGTGTCTAGAATGTT
TTTAAAAATAGGTAGTGGAGCCATAGCCCTCACCATAGACACCTCTGAGCCCACTGGCATTGTCTCTGA
GCAGAAGATGGCTGTGCCACTCACATATGCTAATCTTGGCAAATCTGCCAAGCATGTCTTCACCAAGGG
ATATGGATTTGGCTTAATAAAACCTGATTTGAAAACAAAA
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_003630.3
Synonyms PBD10A; PBD10B; TRG18
Summary The product of this gene is involved in peroxisome biosynthesis and integrity. It assembles membrane vesicles before the matrix proteins are translocated. 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 Zellweger syndrome (ZWS). [provided by RefSeq, Oct 2008]
Locus ID 8504
MW 55.8
*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.

Documents

Customer Reviews 
Loading...