ATR (NM_001184) Human 3' UTR Clone

Specifications

Product Data
Product Name	ATR (NM_001184) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	FCTCS; FRP1; MEC1; SCKL; SCKL1
ACCN	NM_001184
Insert Size	221 bp
Sequence Data	Insert Sequence (showhide) >SC202265 3' UTR clone of NM_001184 The sequence shown below is from the reference sequence of NM_001184. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GCCAGATGTATCTTGGTTGGACTCCATATATGTGAAATGAAATTATGTAAAAGAATATGTTAATAATCTA AAAGTAATGCATTTGGTATGAATCTGTGGTTGTATCTGTTCAATTCTAAAGTACAACATAAATTTACGTT CTCAGCAACTGTTATTTCTCTCTGATCATTAATTATATGTAAAATAATATACATTCAGTTATTAAGAAAT AAACTGCTTTC ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
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_001184.3
Synonyms	FCTCS; FRP1; MEC1; SCKL; SCKL1
Summary	The protein encoded by this gene is a serine/threonine kinase and DNA damage sensor, activating cell cycle checkpoint signaling upon DNA stress. The encoded protein can phosphorylate and activate several proteins involved in the inhibition of DNA replication and mitosis, and can promote DNA repair, recombination, and apoptosis. This protein is also important for fragile site stability and centrosome duplication. Defects in this gene are a cause of Seckel syndrome 1. [provided by RefSeq, Aug 2017]
Locus ID	545

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