FANCA (NM_001018112) Human 3' UTR Clone

Specifications

Product Data
Product Name	FANCA (NM_001018112) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	FA; FA-H; FA1; FAA; FACA; FAH; FANCH
ACCN	NM_001018112
Insert Size	755 bp
Sequence Data	Insert Sequence (showhide) >SC209399 3’UTR clone of NM_001018112 The sequence shown below is from the reference sequence of NM_001018112. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCCTCCACTCACAAGATCGTGAGGTGCTGAGCTTCAGCAGCCCGCTCCTGAGCACACTTCCTCTGCCAG TTACGATAACGTGCGTGAGGAGGAGGCGACCATGGGAAAGCCCGGGGAACGCTCTGGTCAGCCTTTTCC TGTGAGGATGAGGTCGGAAGGTGCGCCCACTGCAGTATCCTGTTCCGCCTCTGGAAGTCCTGCACCAAT GTTTGTCCCACTCACTGTGACCTCCTCCTGTGTGGAGTCTCCCCTTGCTCCTCCTTCCCTGGGTGTGAT TCAGGCTCTAGAGCTGGCCCTGCCTCTCAGCCCCCCACATTTCTAGAACACACTGTAGCTGTGCCTCTA CAGACTCCCGCTGCCTGGCCTCCACAGATCCTGCTCAGATTCACCAGTAGGCAAAGCTTGGCCCTATTA GCTTTTTCTCTCCATGGCTCTGTGGAGATGTGCGGAGACCCTTACAGGTCGGGAGGCGGAAGCTGAGGA GTGGGGGCTGGGTGGAAGGTGGACATCGGGGTTTGGTGGAAATGGGGCTCTGGGGTTTGCTTCCCTCTA GTGTGGGCAGGGGACCTTGAAGTGAAGTCTTGAGAAACCAGTAGAATTTGCCACTGTTTCCAGGCCTTG TCAACCTTTTCATTCTTTATTTTGCTCCTCATTTCCCATCCCTCACAGTAACTGTTTAACTGCTCAATT AAATGTGTTGTACCGTTCGGTACTTTTACTGAAACAGTGAATAAAGCACTGTGTGATTTCCTGAA 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_001018112.3
Synonyms	FA; FA-H; FA1; FAA; FACA; FAH; FANCH
Summary	The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provided by RefSeq, Jul 2008]
Locus ID	2175
MW	27.1

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.