NuMA (NUMA1) (NM_006185) Human 3' UTR Clone

Specifications

Product Data
Product Name	NuMA (NUMA1) (NM_006185) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	NMP-22; NUMA
ACCN	NM_006185
Insert Size	693 bp
Sequence Data	Insert Sequence (showhide) >SC208622 3’UTR clone of NM_006185 The sequence shown below is from the reference sequence of NM_006185. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CCTCGAGCCAAGGGCAAGGCAAAGCACTAAAGGGCCAGTACCAGTGAGTGGCCCCACCTGTGTCCCCGA TGCTGACCTCACCTGGTCCTCCGCCTACTGTCCCTCTCAGTGCCTTCTCTCAGCTCCCAGGCCAACAGT AGCCAAACCCCTAGAGACAGTGATGCCTGCCCGCACCCTGGCCTGGTCCCTGGTCCTTCACTGGCGCCT TCTCGGAGCTGGCCCAGGGGGCCTGGAGCATGGACAGTGTGGGCGCTCTCCCTACCTTGCCTCCTTTTT TCTTAAAGCAAAGTCACTTCTCCATCACAACCAGATTTGAGGCTGGTTTTGATGGCTGGGTCCTTGGGC CTGGCCAGTCTTCCTCTTAGCCTCTGGATCTAGAAGGGACCATAAGAGGAGTAGGCCCTGGTTCCTGCT GTCCTGGTGGCTGGGCCCAGCAGGGGCCCTCACTCTTGAAGTCCAGGACTGGGTCTGACCTGGTGGGAG CACCTGCCAGAGGATGCTCTTTCCCAGGACGGATGGGCCCTATGTCTCAGGAGTGGGGTTGGGGGACAG CCTTCAGCAGCAGCTCACACCCTACCTTCCCCAGACTTGCACTGGGGTGGGATTTGGAGTGATGGGAAG GTTTTTAAGGGCCGGGGATGGATCTTTTCTAAATGTTATTACTTGTAAATAAAGTCTATTTTTCTCCCG TGA 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_006185.4
Synonyms	NMP-22; NUMA
Summary	This gene encodes a large protein that forms a structural component of the nuclear matrix. The encoded protein interacts with microtubules and plays a role in the formation and organization of the mitotic spindle during cell division. Chromosomal translocation of this gene with the RARA (retinoic acid receptor, alpha) gene on chromosome 17 have been detected in patients with acute promyelocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013]
Locus ID	4926
MW	24.7

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