RNF70 (PJA1) (NM_022368) Human 3' UTR Clone

Specifications

Product Data
Product Name	RNF70 (PJA1) (NM_022368) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	PRAJA1; RNF70
ACCN	NM_022368
Insert Size	591 bp
Sequence Data	Insert Sequence (showhide) >SC206216 3’UTR clone of NM_022368 The sequence shown below is from the reference sequence of NM_022368. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TGCCGCTGCATGTTCCCTCCCCCACTCTAAAGACCAAGGCCGTTTACTCCTGGTCTGATTATTTTCCCC ATCTGAAATCCACAATACTGCAGGAGCCCTCTTGAAATTAACAATGGAAATAAAACCAATCAGTCAGTT AGCCTAAACCTATTGATTCCTCGTGATTATTTCCAATGTGAAAACAGTTGTGTATGATTGCATTAAAAA TCATATCATCTTTTAGAGGTTAGAAAAGGGAAAACTAAACTTTCTAAATGCTACTTGAGATTGCAGTAA GAAGATACGTTTTCTAACCTGAAAGTTAAATCGCATTTGTTTTCTTCAGTAGAATGGGAATGTGTTGCT GTTACTTGTAATGTCAAGTTTATCTGTTAAATATGTCCAAAAGGCAAAATCATTTTTGTTGCATGTTAT GGGTCGATGTTCCTGTAATTGCAGTGCCGTAAAAGCTTATTAAAGTTGTTCTTTTGGTTTTACATGGTA TAATGGAATTTTTTGGTTTTGTCTGAAGCAGTGGTACTGAATGACTTTATAATTGATCCCTTGCATTTG CATCAAAAGCTTTAGTTTCACTGGAAATGCTGACTTCAA 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_022368.5
Synonyms	PRAJA1; RNF70
Summary	This gene encodes an enzyme that has E2-dependent E3 ubiquitin-protein ligase activity. This enzyme belongs to a class of ubiquitin ligases that include a RING finger motif, and it can interact with the E2 ubiquitin-conjugating enzyme UbcH5B. This gene is located in an area of chromosome X where several X-linked cognitive disability disorders have been associated, and it has also been found as part of a contiguous gene deletion associated with craniofrontonasal syndrome, though a direct link to any disorder has yet to be demonstrated. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010]
Locus ID	64219
MW	23.2

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