MAX (NM_145114) Human 3' UTR Clone

Specifications

Product Data
Product Name	MAX (NM_145114) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	bHLHd4
ACCN	NM_145114
Insert Size	466 bp
Sequence Data	Insert Sequence (showhide) >SC206505 3’UTR clone of NM_145114 The sequence shown below is from the reference sequence of NM_145114. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GTGCACAAGAAAAAAGAATGCAAGATTTAAAAAATGATTGTTTTGACCCCTTACACAAATGTCTTACTC CTGGCTTTAATTAAGCTGCTTGAGGGCTGATAGCTCTGCCTTACCCTGGTAATCAGCAAAATGGTCCTG TGGCTGGGGAGGCCCTGGCAGCAGGAAGCCTTCAAGGAGCCATGGGTCTGTGCTGACTCTGGCCTTACA ACCTTCCAGCCTCCTTTGCTGGCATTGATGGGGTTCCATTTTTGAATGAACTAGTTTAATGTGGATCCA AATTTATTGTGCATATTCTTTCGTTTTGGTTTTCAAAAGATGGCTTATTCACATGGAAATGTACACCAG TTTAGCCCTGGGCCCTCCCTTTACCTTCATATGTGTAAAAGCTTACACAGGTTTCAGAAAATAAATGGT TTCATTTTCTCTAAAATAACTAGTACAAAATAAAACAGATGTCAGTTGTTGA 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_145114.3
Synonyms	bHLHd4
Summary	The protein encoded by this gene is a member of the basic helix-loop-helix leucine zipper (bHLHZ) family of transcription factors. It is able to form homodimers and heterodimers with other family members, which include Mad, Mxi1 and Myc. Myc is an oncoprotein implicated in cell proliferation, differentiation and apoptosis. The homodimers and heterodimers compete for a common DNA target site (the E box) and rearrangement among these dimer forms provides a complex system of transcriptional regulation. Mutations of this gene have been reported to be associated with hereditary pheochromocytoma. A pseudogene of this gene is located on the long arm of chromosome 7. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
Locus ID	4149
MW	17.9

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