ARHGEF7 (NM_003899) Human Untagged Clone

CAT#: SC117668

ARHGEF7 (untagged)-Human Rho guanine nucleotide exchange factor (GEF) 7 (ARHGEF7), transcript variant 1


  "NM_003899" in other vectors (6)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol ARHGEF7
Synonyms BETA-PIX; COOL-1; COOL1; Nbla10314; P50; P50BP; P85; P85COOL1; P85SPR; PAK3; PIXB
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC117668 sequence for NM_003899 edited (data generated by NextGen Sequencing)
ATGACCGACAATAGCAACAATCAACTGGTAGTAAGAGCAAAGTTTAACTTCCAGCAGACC
AATGAGGACGAGCTTTCCTTCTCAAAAGGAGACGTCATCCATGTCACCCGTGTGGAAGAG
GGAGGCTGGTGGGAGGGCACACTCAACGGCCGGACCGGCTGGTTCCCCAGCAACTACGTG
CGCGAGGTCAAGGCCAGCGAGAAGCCTGTGTCTCCCAAATCAGGAACACTGAAGAGCCCT
CCCAAAGGATTTGATACGACTGCCATAAACAAAAGCTATTACAATGTGGTGCTACAGAAT
ATTTTAGAAACAGAAAATGAATATTCTAAAGAACTTCAGACTGTGCTTTCAACGTACCTA
CGGCCATTGCAGACCAGTGAGAAGTTAAGTTCAGCAAACATTTCATATTTAATGGGAAAT
CTAGAAGAAATATGTTCTTTCCAGCAAATGCTCGTACAGTCTTTAGAAGAATGCACCAAG
TTGCCCGAAGCTCAGCAGAGAGTCGGAGGCTGCTTTTTAAACCTGATGCCACAGATGAAA
ACCCTGTACCTCACGTATTGTGCCAATCACCCTTCTGCAGTGAATGTCCTCACGGAACAC
AGTGAGGAGTTGGGGGAGTTCATGGAGACCAAAGGTGCCAGCAGCCCTGGGATTCTCGTG
CTGACCACGGGCCTGAGCAAACCCTTCATGCGCCTGGATAAATACCCTACGCTGCTCAAA
GAGCTCGAGAGACACATGGAGGATTATCATACAGATAGACAAGATATTCAAAAATCCATG
GCTGCCTTCAAAAACCTTTCAGCCCAATGTCAAGAAGTCCGGAAGAGGAAAGAGCTTGAG
CTGCAGATCCTGACGGAAGCCATCCGGAACTGGGAGGGCGATGACATTAAAACTCTGGGC
AACGTCACTTACATGTCCCAGGTCCTGATTCAGTGTGCCGGAAGTGAGGAAAAGAATGAA
AGATATCTTCTACTCTTCCCAAATGTTTTGCTAATGTTGTCTGCCAGTCCTAGGATGAGT
GGCTTTATCTATCAGGGAAAGCTTCCAACGACAGGAATGACAATCACAAAGCTTGAGGAC
AGTGAAAATCATAGAAATGCATTTGAAATATCAGGGAGCATGATTGAGCGGATATTAGTG
TCGTGCAACAACCAGCAGGATCTGCAGGAATGGGTGGAGCACCTACAGAAGCAAACGAAG
GTCACGTCTGTGGGAAACCCCACCATAAAGCCTCATTCAGTGCCATCTCATACCCTCCCC
TCCCACCCGGTCACTCCGTCCAGCAAGCACGCAGACAGCAAGCCCGCGCCGCTGACGCCC
GCCTACCACACGCTGCCCCACCCCTCCCACCACGGCACCCCGCACACCACCATCAACTGG
GGACCCCTGGAGCCTCCGAAAACACCCAAGCCCTGGAGCCTGAGCTGCCTGCGGCCCGCG
CCTCCCCTCCGGCCCTCAGCTGCTCTCTGCTACAAGGAGGATCTTAGTAAGAGCCCTAAG
ACCATGAAAAAGCTGCTGCCCAAGCGCAAACCTGAACGGAAGCCTTCAGATGAGGAGTTC
GCGTCCCGGAAAAGCACAGCTGCTTTGGAAGAAGATGCTCAGATTCTGAAAGTCATTGAA
GCTTACTGCACCAGCGCCAAAACAAGGCAAACACTCAATTCAAGTTCACGCAAAGAATCT
GCTCCACAAGTTTTGCTTCCAGAAGAAGAGAAAATTATAGTGGAAGAAACTAAAAGTAAT
GGTCAGACAGTGATAGAAGAAAAGAGTCTTGTGGATACCGTATATGCATTAAAGGATGAA
GTTCAAGAATTAAGACAGGACAACAAAAAGATGAAGAAATCTCTAGAGGAAGAACAGAGA
GCCCGCAAAGACCTGGAGAAGCTGGTGAGGAAAGTCCTGAAGAACATGAATGATCCTGCC
TGGGATGAGACCAATCTATAA

Clone variation with respect to NM_003899.3
9 t=>c
>OriGene 5' read for NM_003899 unedited
CGTTANCATTTGTATACGACTCATATAGGCGGCCGCGAATTCGGCACGAGGGCAAACCGT
TACGTGGCTCATCACTCTGGGGGTGCTGGAGTCGCCCAAAAAAACCATCTCGGACCCGGA
GGGCTTTCTGCAGGCGTCGCTGAAGGATGGGGTGGTCCTCTGCAGGCTGCTGGAGCGCCT
GCTCCCCGGGACCATCGAGAAAGTCTACCCCGAGCCCCGGAGCGAGAGCGAGTGCCTGAG
CAACATCCGCGAGTTCCTGCGCGGCTGCGGGGCTTCCCTGCGGCTGGAGACGTTTGATGC
AAATGATTTGTATCAGGGGCAGAATTTTAACAAGGTCCTCAGTTCCTTAGTGACTCTAAA
TAAAGTAACAGCAGACATCGGGCTGGGGAGTGACTCCGTGTGTGCCCGGCCCTCGTCTCA
CCGCATAAAGTCTTTTGACTCCCTTGGATCACAGTCTTTGCACACTCGGACTTCAAAACT
GTTCCAGGGCCAGTATCGGAGTTTGGACATGACCGACAATAGCAACAATCAACTGGTAGT
AAGAGCAAAGTTTAACTTCCAGCAGACCAATGAGGACGAGCTTTCCTTCTCAAAGGAGAC
GTCATCCATGTCACCCGTGTGGAATAGGAGGCTGTGGNGGAAGGGCACACTCAACGGCCG
GACCGGCTGGTTCCCAGCAACTACGTGCGCGAGGTCAAGGCCAGCGAGAAGCCTGTGTCT
CCCATATCATGACACTGAAGAGCCCTCCAAAGGATTTGATACGACTGCCATANNACAAAC
ATTACAATGTGGTGCTACAGAATATTTTAGAAACAGATNATGAATATTCTAAAGAATTNC
AGACTGTGCTTTTCACGTACCTACGGCCATTGCAGACANTGGAAAAAAGTTAAGTTCAGC
ANACATTTCTNATTTAATGGNGAATNCTAGAAGAATTAATGCCCCTT
>OriGene 3' read for NM_003899 unedited
TGCTCTGGACCGGCGGCCGCAATCTAGGGTCGAGTTTTTTTTTTTTTTTTTTTTTTTTTG
ACATAAGAAAAAAATCAGTTTAATAATTACAACAGTGTAGCATCAACATTGTAGTAGTCA
ACACTAGGACATTGTCTGTGACATTTAAATTAGGAGTTTCTCCACACTTGTCAACAGGCG
CCCTGGGTGTCCCAGAGAAGTGAAGAAATGATTGGCATTAAGGAGTCCACACAACCAGGG
CAGGCATTCAAGGTCCCAGACGCCCAGTGCATGTGGACAAGCACAGACGCCACTGAGTGT
GAAGGAACGAGCTTCTGATGCTACATTCCAACATCGCTGAAAACTGAAAGTGCTTCACAT
CTACAGGATAAGAAATGGCTTCATCTCCTCATCCATACAAGGTGAGAGCAAAGGAGTAAC
CCTCGGGCAAATCGTGGCCCCTTTAAACGTTTATATCAAGTTCCCACCCCCTTGGGAGGT
CACACGGTGAAACAGACACAGTTATATACAACAGGGCAGGTTTTTAAAAAGAGTTGCTCT
CAGACGCATTTTTCCTGCTCCCTAAAAAGCCGAGGAAGATACTGGATCCACAGAAAGAAA
AGGCAATGCCGTAACATGAGGCCCTCATGGCCGCACCGTCCAGGGGAAGGGCTGNTAAAA
ACACAAGTATTCTTGTNGAATACTTCGATCTGAGCATTAAGGCAGGTCTGCAGGAGATCC
GTCCTGGGGACTCCGACAGCAACGCTACCGGCTTCGAGAGGACAGTTAATGTCGCCCTCC
CGCAGAGGGGCCGAGAGATCAAACAAGAGTTGTTCCTGAGTTAAAAACTGCTACACAGCA
AACTCCCATAACTCAAGGTGAATGTTTTCCACTGGCATGCTTTACGCATACCAAAAATAA
CTTGTAAACTCAGCCTACCAAAAGAAGTGTTGACTCTGCTGGGCCCCCTGATGAATAACC
GCTAN
Restriction Sites NotI-NotI     
ACCN NM_003899
ORF Size 1941 bp
Insert Size 5130
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Reference Data
RefSeq NM_003899.2, NP_003890.1
RefSeq Size 5032
RefSeq ORF 1941
Locus ID 8874
Domains RhoGEF, SH3, PH
Protein Pathways Regulation of actin cytoskeleton
Gene Summary This gene encodes a protein that belongs to a family of cytoplasmic proteins that activate the Ras-like family of Rho proteins by exchanging bound GDP for GTP. It forms a complex with the small GTP binding protein Rac1 and recruits Rac1 to membrane ruffles and to focal adhesions. Multiple alternatively spliced transcript variants encoding different isoforms have been observed for this gene. [provided by RefSeq, Mar 2016]
Transcript Variant: This variant (1) differs in the 5' UTR, lacks a portion of the 5' coding region, and contains a different 3' coding region and 3' UTR, compared to variant 1. It initiates translation at a downstream start codon. Variants 1, 5, 6, 18, and 19 all encode isoform a (also known as p85Cool-1), which has a shorter N-terminus and a longer and distinct C-terminus, compared to isoform c. Sequence Note: The RefSeq transcript and protein were derived from genomic sequence to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on alignments.

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