FGD1 (NM_004463) Human 3' UTR Clone

Specifications

Product Data
Product Name	FGD1 (NM_004463) Human 3' UTR Clone
Vector	pMirTarget
Synonyms	AAS; FGDY; MRXS16; ZFYVE3
ACCN	NM_004463
Insert Size	685 bp
Sequence Data	Insert Sequence (showhide) >SC208727 3’UTR clone of NM_004463 The sequence shown below is from the reference sequence of NM_004463. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GAATCCCCCCAGACCCGAGACAAGACCTAGAGGGTTTGGGACAAACTGGGAGCCCCCACCCCACACTCT AGTTGCCCATGTCTGATTGGGGGCTCTAGCCCCTTCCCTCCCAGCTCAGTCAATACTTGAACTCCCATC ACGGGCACTTTCAATCCCGAATGCTGGGTCTTGGGTTTTTTAATTCATCTTTTCACAAAACGTGGGCTT TTAAAAAATATATTCCTACAGTGATGTCAATTTTTATTAATCCCTGTCCCCAGGGAGGGTGGGAGCCGT TGCCAGTCCTACCTGAATTAGGTCGTTTTTCTCCCTCATCCCTCAATACCCTACCACAGATCCTGCCTC CACCCAGTTCCCCACAAAGCACCAGAGGTAGGAGACCTGGATTCAAGTGCCAGCTCTGCCACTGACCCT GGGGCCCCGACCCAGCCCTGCCTCCTCAGCCAGTGTCTTCACACGTACAACTCCACGTGGGGTGGCAAC TAGACCTCTCCTGCCTCTCCCATGGCTTACAGCTTCTACCCGGCCCCAAGGCTACCCAGTATTTTATCG TCCAGACCCATGGCAGGGCCAGCGGGCAGGACAGGGAAACAGGGGGGAGGACAATGGATACTCAGTTTT TTGTGTTTTTTTGTGTGTTTTTTTTTTTTTAAGAAAAATACAGTTTATTTCAGGCTTACAGTAA 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_004463.3
Synonyms	AAS; FGDY; MRXS16; ZFYVE3
Summary	This gene encodes a protein that contains Dbl (DH) and pleckstrin (PH) homology domains and is similar to the Rho family of small GTP-binding proteins. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs and can stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. Defects in this gene are the cause of the faciogenital dysplasia in Aarskog-Scott syndrome and a syndromatic form of X-linked cognitive disability. [provided by RefSeq, Jul 2017]
Locus ID	2245
MW	25

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