Complement C7 (C7) (NM_000587) Human 3' UTR Clone

Specifications

Product Data
Product Name	Complement C7 (C7) (NM_000587) Human 3' UTR Clone
Vector	pMirTarget
ACCN	NM_000587
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC214316 3’UTR clone of NM_000587 The sequence shown below is from the reference sequence of NM_000587. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC ATAAGGCCTTGTGCTGCGGAAACCCAGTAGGCTCCTGGAGGCCCTGGTCAGCTTGCTTGGAATCCAGCA GGCAGCTGGGGCTGAGTGAAAACATCTGCACAACTGGGCACTGGACAGCTTTTCCTTCTTCTCCAGTGT CTACCTTCCTCCTCAACTCCCAGCCATCTGTATAAACACAATCCTTTGTTCTCCCAAATCTGAATCGAA TTACTCTTTTGCCTCCTTTTTAATGTCAGTAAGGATATGAGCCTTTGCACAGGCTGGCTGCGTGTTCTT GAAATAGGTGTTACCTTCTCTGGGCCTTGGTTTTTTAAAATCTGTAAAATTAGAGGATTGCACTAGAGA AACTTGAATGCTCCATTCAGGCCTATCATTTTATTAAGTATGATTGACACAGCCCATGGGCCAGAACAC ACTCTACAAAATGACTAGGATAACAGAAAGAACGTGATCTCCTGATTAGAGAGGGTGGTTTTCCTCAAT GGAACCAAATATAAAGAGGACTTGAACAAAAATGACAGATACAAACTATTTCTATCCTGAGTAGTAATC TCACACTTCATCCTATAGAGTCAACCACCACAGATAGGAATTCCTTATTCTTTTTTTAATTTTTTTAAG ACAGAGTCTCACTTTGTTGCCCAGGCTGGAGCGCAGTGGGGTGATCTCATCTCCCTGCAACCTCCGCCT CCTGGGTTCAAGCGATTCTTGTGCCTCAGCTTCCCAAGCAGCTGGGATTACAGGTGCCCGCCACCACGC CCAGCTAATTTTTGCATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCACGCTCGTCTCCAACTCCT GACCTCAGGTAATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAACCACCACGCCTG GCTGGAATACTTACTCTTGTCGGGAGATTGAACCACTAAAATGTTAGAGCAGAATTCATTATGCTGTGG TCACAGGGGTGTCTTGTCTGAGAACAAATACAATTCAGTCTTCTCTTTGGGGTTTTAGTATGTGTCAAA CATAGGACTGGAAGTTTGCCCCTGTTCTTTTTTCTTTTGAAAGAACATCAGTTCATGCCTGAGGCATGA GTGACTGTGCATTTGAGAATAGTTTTCCCTATTCTGTGGATACAGTCCCAGAGTTTTCAGGGAGTACAC AGGTAGATTAGTTTGAAGCATTGACCTTTTATTTATTCCTTATTTCTCTTTCATCAAAACAAAACAGCA GCTGTGGGAGGAGAAATGAGAGGGCTTAAATGAAATTTAAAATAAGCTATATTATACAAATACTATCTC TGTATTGTTCTGACCCTGGTAAATATATTTCAAAACTTCAGATGACAAGGATTAGAACACTCATTAAAG ATGCTATTCTTCAGAATTGTTTCATTTGTATGATGTTTCATTTTAGAGAAGATTTTCATGATGAATGGT TAATGTGTTCTTGCCTGAAGTTTTATGTCTGATCCAGATCTAGCTTTTTGTATCAAAGTGTGCCCTAAG GGAAGATGCAGATATAATATGTTGAAGTTACAAGGAGGCAGGTTTCAATTGGTTAAAAACAATGACATT CAGACATTGCAACTGCATTTGTTAGCGGTTATTACAGAGTTAATTTCTACCCTGGATGGGAGGACACAT TTGAACATGCTAGGCCTGGATGCAGACCCTGAGACAAAAGGTTGAACAAGTAATTCATTTGGAAGGAAA TACCTCAGTATCCTTCCAATAATTTCTCCTCTTAGCTTAAGCTAGTATGGAGTTAGATTCCTACCGCTT ATGTATCACCATGCCCCCTTCCTAAATAATACAGAGGATATGGTCAGCATTATCACATATCATCAGAGA TTGAGGTTTGAAAGAAAGGAAATGAGTAGATGTAACTAAGAGGTTTGAGAAAGGAATTTCAGCAGAGTT ATTGAAGGAGAAGTCAAGGAGAGGAGAAGGAGAGGAGCAGTGAATGTTGTCGTGAAGAGGTGTTGTCT 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_000587.4
Summary	This gene encodes a serum glycoprotein that forms a membrane attack complex together with complement components C5b, C6, C8, and C9 as part of the terminal complement pathway of the innate immune system. The protein encoded by this gene contains a cholesterol-dependent cytolysin/membrane attack complex/perforin-like (CDC/MACPF) domain and belongs to a large family of structurally related molecules that form pores involved in host immunity and bacterial pathogenesis. This protein initiates membrane attack complex formation by binding the C5b-C6 subcomplex and inserts into the phospholipid bilayer, serving as a membrane anchor. Mutations in this gene are associated with a rare disorder called C7 deficiency. [provided by RefSeq, Nov 2016]
Locus ID	730
MW	76.2

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