SP140 (NM_007237) Human 3' UTR Clone

Specifications

Product Data
Product Name	SP140 (NM_007237) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	LYSP100; LYSP100-A; LYSP100-B
ACCN	NM_007237
Insert Size	561 bp
Sequence Data	Insert Sequence (showhide) >SC207376 3’UTR clone of NM_007237 The sequence shown below is from the reference sequence of NM_007237. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GCTATTCAGGAAACAAATGGGAACAATTGACTGGATTAGTGGATGCTGAAAGCATTCAGCAAATGGCAC CCTAAAATATGCCGCTGGTTTGCCACTGACTTCAAAATGAGGTCACTTGGGCACAGCACATGCAGGGAG GGGCTTTTCTCTGAGCCTCCTTCATCTGCCCAAAGACAAATCCTCAAAAGGAAATTCAATCATCATGAA TCACAACCCCAAGTATCTCATCAGCCAGGGAAGAGTAAGTGGGATCACAGGGAAGGATGTTGGCAGCGA CACCATCCCATACAGGCTCTTACCTCTTCTCCTGAGGGCTGCTCCAGACAACATTTATTACCCAGAAGA CCTTTTGTCTGAAAACCAGCCAAGCTTTATTCAGGACACACTTCTTGCCTTCACTTTCCCACTTCCGTG GCCACCTCCATGCAGAAGCCCTAAGCCCACATTCTTTCGATAGCTCACGGTGGTGCATGAGTGTCCATC ATCTGACTCTTCTCGGAGTCTCATATTTTGTGGGACTCCTGTGCAAACATATGTTATTAAAATTTTTTT CCTCCTGTT 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_007237.5
Synonyms	LYSP100; LYSP100-A; LYSP100-B
Summary	This gene encodes a member of the SP100 family of proteins, which are share common domains including an N-terminal homogeneously staining region domain followed by a SP100/autoimmune regulator/NucP41/P75/deformed epidermal autoregulatory factor domain, a plant homeobox zinc finger, and a bromodomain. The encoded protein is interferon-inducible and is expressed at high levels in the nuclei of leukocytes. Variants of this gene have been associated with multiple sclerosis, Crohn's disease, and chronic lymphocytic leukemia. Alternative splicing results in multiple variants. [provided by RefSeq, Aug 2016]
Locus ID	11262
MW	21.4

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