NSDHL (NM_015922) Human 3' UTR Clone

CAT#: SC203332

3' UTR clone of NAD(P) dependent steroid dehydrogenase-like (NSDHL) transcript variant 1 for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


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

CNY 1,280.00

Specifications

Product Data
Product Name NSDHL (NM_015922) Human 3' UTR Clone
Vector pMirTarget
Synonyms H105E3; SDR31E1; XAP104
ACCN NM_015922
Insert Size 643 bp
Sequence Data
>SC203332 3’UTR clone of NM_015922
The sequence shown below is from the reference sequence of NM_015922. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
AGCTTTCGCCACCTGCGGAGGGTCAAGTGAGGGACACTGGAGGCTGGGCTCTCTCGACACGTTGCTCAG
CCAGTCACTCCTTCCCCTGTGGATTGATGAAATAACATCCTTTGAATGAGTTTGCTCTGAGCCTGTGAC
TCCTTCTGCTAGGCAGAGAGCGCACCCTACTCTTTCCGTGACGATGAGGGCGGCAAAAACAGACATTTC
TTCCTTCATGGAACTGGATTTGGATTTCTTGAAGCAGGCAGCTTCATATTATACCGATTTGTTCTCTGT
CTTTTTGTGTCTCTCTGTTTACCCCCTCCCTTGCCCCCTCTTCTGGTTTATACATTTCATTCCAGTGTC
CTTGTACATAATCAAGGAAGCTGTAGGAAGCTACAACCCATTTGTTAGTTCTGATGGAGAACCATTTCC
ATGCAGACCAATACTAGAGTGAAGCCTCTAGACTTTGTTCAAGATACTCTATCTTCAAAATATCCCAGA
AGAAAAACAGAAGCTGTTAACACACAGGTGAGACTTTACATATACATTTCATACTGACAGTGAGCTTAG
AGCAAAAGCTGAAAGCTGAAATGACTGTAATTCCTCCCCAGTCTCTGTTGCTTGTTCAACTCCTTACAT
GTTCCACATTCTCTTTCAGGTA
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_015922.3
Synonyms H105E3; SDR31E1; XAP104
Summary The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008]
Locus ID 50814
MW 24.3
*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.

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