FGF13 (NM_001139500) Human 3' UTR Clone

Specifications

Product Data
Product Name	FGF13 (NM_001139500) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	DEE90; FGF-13; FGF2; FHF-2; FHF2; LINC00889
ACCN	NM_001139500
Insert Size	2000 bp
Sequence Data	Insert Sequence (showhide) >SC213831 3’UTR clone of NM_001139500 The sequence shown below is from the reference sequence of NM_001139500. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC AAATCCATGAGCCACAATGAATCAACGTAGCCAGTGAGGGCAAAAGAAGGGCTCTGTAACAGAACCTTA CCTCCAGGTGCTGTTGAATTCTTCTAGCAGTCCTTCACCCAAAAGTTCAAATTTGTCAGTGACATTTAC CAAACAAACAGGCAGAGTTCACTATTCTATCTGCCATTAGACCTTCTTATCATCCATACTAAAGCCCCA TTATTTAGATTGAGCTTGTGCATAAGAATGCCAAGCATTTTAGTGAACTAAATCTGAGAGAAGGACTGC CAAATTTTCTCATGATCTCACCTATACTTTGGGGATGATAATCCAAAAGTATTTCACAGCACTAATGCT GATCAAAATTTGCTCTCCCACCAAGAAAATGTAAAAGACCACAATTGTTCTTCAAAAACAAACAAAACA AAACAAAACAAAATTAACTGCTTAAATGTTTTGTCGGGGCAAACAAAATTATGTGAATTGTGTTGTTTT CTTGGCTTGATGTTTTCTATCTACGCTTGATTCACATGTACTCTTTTCTTTGGCATAGTGCAACTTTAT GATTTCTGAAATTCAATGGTTCTATTGACTTTTTGCGTCACTTAATCCAAATCAACCAAATTCAGGGTT GAATCTGAATTGGCTTCTCAGGCTCAAGGTAACAGTGTTCTTGTGGTTTGACCAATTGTTTTTCTTTCT TTTTTTTTTTTTTTAGATTTGTGGTATTCTGGTCAAGTTATTGTGCTGTACTTTGTGCGTAGAAATTGA GTTGTATTGTCAACCCCAGTCAGTAAAGAGAACTTCAAAAAATTATCCTCAAGTGTAGATTTCTCTTAA TTCCATTTGTGTATCATGTTAAACTATTGTTGTGGCTTCTTGTGTAAAGACAGGAACTGTGGAACTGTG ATGTTGTCTTTTGTGTTGTTAAAATAAGAAATGTCTTATCTGTATATGTATGAGTCTTCCTGTCATTGT ATTTGGCACATGAATATTGTGTACAAGGAATTGTTAAGACTGGTTTTCCCTCAACAACATATATTATAC TTGCTACTGGAAAAGTGTTTAAGACTTAGCTAGGTTTCCATTTAGATCTTCATATCTGTTGCATGGAAG AAAGTTGGGTTCTTGGCATAGAGTTGCATGATATGTAAGATTTTGTGCATTCATAATTGTTAAAAATCT GTGTTCCAAAAGTGGACATAGCATGTACAGGCAGTTTTCTGTCCTGTGCACAAAAAGTTTAAAAAAGTT GTTTAATATTTGTTGTTGTATACCCAAATACGCACCGAATAAACTCTTTATATTCATTCAAAGAATAAT CTTCCAACATGTATTTATTGAGCGTCCATTATGTGCCAGTAACTGAAGTAGCAACTGGAAGTAAACATT GTATAATGCAGATAAGGTCACTGTCCTCAGATAGTCTACAGTCTAGAGAGTCATATTAACATGAACACT TTAAAGTGTGTTTATTTTACTAGTTACTGTACTTGCACTTCAGATTGGTACAAAGGAATTCACATTCCC GTTCAGTAGTCAAATTATACAAATGAGGCGTTTGTGCTAGTATTTTCTCTGCCACTCACAGTGTCATTT CCCCTCTCTGTTGCTTATTTCTCTCCTCTCTAGAGGGAATACACAGGACTAAATAGTGTCCTTTCTACC TTTGAGAACTGAAGGAAAATGTAAATTTTTTTAAATGTTGATGACTTTTCTCTAGCTCCCCAAAGCTGC ATTGTCTGGCAATGAACACTTTGAGAACAGTCAATACAGATGGTCTCTGACTTACAGTAGTTCAACTTA CATTTTTTCGGGGGCTTTACAGTGGTACAGAAGCAATAGGCATTTAGTAGAACTCATACTTTACCATAC AACCATTTTGCTTTTTATTTCCAGTACACTATTCAATAAATGACATGAGCTATTCAACACTTTTTAATT ACAAAATTTGCTTTGTAGTACATGATTTTGTCCAACTGTAAGCTAATATAAGCGTTCTAAGCACATTT 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_001139500.2
Synonyms	DEE90; FGF-13; FGF2; FHF-2; FHF2; LINC00889
Summary	The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked cognitive disability mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq, Nov 2008]
Locus ID	2258
MW	77.2

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