FANCB (NM_001018113) Human 3' UTR Clone

Specifications

Product Data
Product Name	FANCB (NM_001018113) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	FA2; FAAP90; FAAP95; FAB; FACB
ACCN	NM_001018113
Insert Size	192 bp
Sequence Data	Insert Sequence (showhide) >SC201557 3’UTR clone of NM_001018113 The sequence shown below is from the reference sequence of NM_001018113. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TTTGCTGCACAGAAACTGAGTAATTTATAATTATAATTTCAATTTGATCATATTTTAAAATATGTTTTC ACCACCATATAAGATTTTGGTTCTACTTGCTATATGCCTCCTTTGTAAAAATAAACACCGAGGCTTACT GTAGTAGAAACTTTAGTTTTGATGATGCACAAAATAAACAGCAGTGGTTCTCAA 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_001018113.3
Synonyms	FA2; FAAP90; FAAP95; FAB; FACB
Summary	This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]
Locus ID	2187
MW	7.3

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