CPAMD8 (NM_015692) Human 3' UTR Clone

Specifications

Product Data
Product Name	CPAMD8 (NM_015692) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	ASGD8; K-CAP; VIP
ACCN	NM_015692
Insert Size	187 bp
Sequence Data	Insert Sequence (showhide) >SC201642 3’UTR clone of NM_015692 The sequence shown below is from the reference sequence of NM_015692. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGGATGTCAAACACCTGCACCTTGAGATAATCCTACAACCACATGCAGTTGTGGGACCGCAGTTTGGTC CTGGGGACCATTCATACCCACACACCCAGCTTGTGCCTGTGGTTAACATCTCAGAAAACTCTGGTAAAT GATCACTCCAGGATATTGACAAGAATACACGTTACTGATCTTACTCACA 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_015692.5
Synonyms	ASGD8; K-CAP; VIP
Summary	This gene encodes a member of the protease inhibitor I39 (alpha-2-macroglobulin) family of proteins. These proteins are important in innate and acquired immunity. The encoded protein is membrane-associated and proteolytically processed to generate two chains. Mutations in this gene cause a form of anterior segment dysgenesis, a developmental disorder of the eye. [provided by RefSeq, May 2017]
Locus ID	27151
MW	7.3

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