FCP1 (CTDP1) (NM_004715) Human 3' UTR Clone

Specifications

Product Data
Product Name	FCP1 (CTDP1) (NM_004715) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	CCFDN; FCP1
ACCN	NM_004715
Insert Size	743 bp
Sequence Data	Insert Sequence (showhide) >SC209457 3’UTR clone of NM_004715 The sequence shown below is from the reference sequence of NM_004715. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTGGAGGCGGAGCTCAACGACCTCATGTGAGCGCGGGCAGCGGGCAGGGACTGAAGCCTGACCGACCTC CAGCAGCACTCGGACGTCCCCGGACCAGCCCTCAGTCTCGGTCCACGCTGCTTTCTTCCCAAAGGACAT GTATATTTGCAGAGCTCCACATACAGAAACACATTATTTTGCAGAAATAGGTGTTTTTAAGAAGTTTTA CTACAGGAATGTCTACTTTTGTAAGTGACAGGTGTTAAAGGCCCAGGTGTGCTGTGCCAAAGAGCTCAG CAGAGGCTCACGTGGCCCAGGCTGGTGCGCCCGCTGTCTCGGTAAGGGGCGGGTTGGTGTGTTTTCCCC TTGTGTACCAGAGCACATTCCTTAGGGGACGGCTTTGGGGGTCCCACGAGACATGGACTAGGAGTTTAA GCAGGACAGTGTGCGTGCACGAGCTCCGAGCCCAGCACAGACATGCCTGGAACCCCCGCCGCCTGCTGC TCCCTCCTAGGGAACCCATTTCCGGGGAACGCCGTGACTGTCGGGCAGCCTGGAGCTTCCTGCAGCCTC CTACGCAGGGTCCACGCCACGTGGCCTGGGCTGCCATCCTGCCGTCCTCCCACTGGCATCCTGGCAAGG GGGCGTTGCTTTTCCTGGGCGGCCTTTTATGTCTTGGAGACACCTGATGTAAAGTTTCTGTAAATCTAT TTCATATCTGACCCACCAAACAGATTTCTCTTTAATAAAAATCCTTTTTGTAA 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_004715.5
Synonyms	CCFDN; FCP1
Summary	This gene encodes a protein which interacts with the carboxy-terminus of the RAP74 subunit of transcription initiation factor TFIIF, and functions as a phosphatase that processively dephosphorylates the C-terminus of POLR2A (a subunit of RNA polymerase II), making it available for initiation of gene expression. Mutations in this gene are associated with congenital cataracts, facial dysmorphism and neuropathy syndrome (CCFDN). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011]
Locus ID	9150
MW	26.8

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