MAGED2 (NM_014599) Human 3' UTR Clone

Specifications

Product Data
Product Name	MAGED2 (NM_014599) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	11B6; BARTS5; BCG-1; BCG1; HCA10; MAGE-D2
ACCN	NM_014599
Insert Size	173 bp
Sequence Data	Insert Sequence (showhide) >SC201574 3’UTR clone of NM_014599 The sequence shown below is from the reference sequence of NM_014599. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC TCTGGTGCCTGTGGTTTCTCCTACAAGTGAGATTTTAGATATTGTTAATCCTGCCAGTCTTTCTCTTCA AGCCAGGGTGCATCCTCAGAAACCTACTCAACACAGCACTCTAGGCAGCCACTATCAATCAATTGAAGT TGACACTCTGCATTAAATCTATTTGCCATTTCTGA 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_014599.6
Synonyms	11B6; BARTS5; BCG-1; BCG1; HCA10; MAGE-D2
Summary	This gene is a member of the MAGED gene family. The MAGED genes are clustered on chromosome Xp11. This gene is located in Xp11.2, a hot spot for X-linked intellectual disability (XLID). Mutations in this gene cause a form of transient antenatal Bartter's syndrome. This gene may also be involved in several types of cancer, including breast cancer and melanoma. The protein encoded by this gene is progressively recruited from the cytoplasm to the nucleoplasm during the interphase and after nucleolar stress and is thus thought to play a role in cell cycle regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017]
Locus ID	10916
MW	6.2

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