NSDHL (NM_015922) Human 3' UTR Clone

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	Insert Sequence (showhide) >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

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