FANCD2 (NM_033084) Human 3' UTR Clone

Specifications

Product Data
Product Name	FANCD2 (NM_033084) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	FA-D2; FA4; FACD; FAD; FAD2; FANCD
ACCN	NM_033084
Insert Size	423 bp
Sequence Data	Insert Sequence (showhide) >SC209164 3’UTR clone of NM_033084 The sequence shown below is from the reference sequence of NM_033084. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTTCTATGCCCATTTCCATTCCCTCCATAACAGCTTCTGTGCTTATATAATTTTTGGGACCCAGAAGAA ACAACGACACAATCTTAGAATCACTCCTGAGTATCTCGAGTTGTGGCATTTGTTATAGAGTTGACAATT TTCTGCATTATAGCCTCTCATTTTCCATGAATTCATATCTGAAACCATTTTAGAAGGGAGAAGTCATCG AAGTATTTTCTGAGTGTTGAGAAGAATGAGTTAAACCATTTAAACACATTTGAAACATACAAAAATAGA AATGTGAAAGCATTTGGTGAAAGCCAAAGCACAGAGTCAGAAGCTGCCACCTTAGAGAACTGAAATAAA AATAGAAGTTCTTACGCTTTTTTGTGGTACAGATGCTTTCGACAATTTAAAGAAAGCTAAATAAAAATG TAGACATGG 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_033084.6
Synonyms	FA-D2; FA4; FACD; FAD; FAD2; FANCD
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 D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Locus ID	2177
MW	16.8

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