RLTPR (CARMIL2) (NM_001013838) Human 3' UTR Clone

Specifications

Product Data
Product Name	RLTPR (CARMIL2) (NM_001013838) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CARMIL2b; IMD58; LRRC16C; RLTPR
ACCN	NM_001013838
Insert Size	81 bp
Sequence Data	Insert Sequence (showhide) >SC200404 3’UTR clone of NM_001013838 The sequence shown below is from the reference sequence of NM_001013838. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GACCAAAGAGGCGGCGGCCCCAATCCCTGATCCTCTCCTCTCCTGCCGCATGAGATTATTTTATTAAAA AACTCAAAGGAA 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_001013838.3
Synonyms	CARMIL2b; IMD58; LRRC16C; RLTPR
Summary	This gene encodes a member of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with and negatively regulates the heterodimeric capping protein and promotes cell migration. Reduced expression of this gene has been observed in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized by smooth muscle tumors and impaired T-cell function. [provided by RefSeq, May 2017]
Locus ID	146206
MW	2.9

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