TBC1D15 (NM_001146214) Human Untagged Clone

CAT#: SC327168

TBC1D15 (untagged)-Human TBC1 domain family member 15 (TBC1D15) transcript variant 2


  "NM_001146214" in other vectors (4)

Reconstitution Protocol

USD 1,390.00

5 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol TBC1D15
Synonyms RAB7-GAP
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>NCBI ORF sequence for NM_001146214, the custom clone sequence may differ by one or more nucleotides
ATGTGTCCAGGACTTTATCCATACTCCAGTTTGTTGGAGTATGGTAGGAGTATGATTATA
TATGAACAAGAAGGAGTATATATTCACTCATCTTGTGGAAAGACCAATGACCAAGACGGC
TTGATTTCAGGAATATTACGTGTTTTAGAAAAGGATGCCGAAGTAATAGTGGACTGGAGA
CCATTGGATGATGCATTAGATTCCTCTAGTATTCTCTATGCTAGAAAGGACTCCAGTTCA
GTTGTAGAATGGACTCAGGCCCCAAAAGAAAGAGGTCATCGAGGATCAGAACATCTGAAC
AGTTACGAAGCAGAATGGGACATGGTTAATACAGTTTCATTTAAAAGGAAACCACATACC
AATGGAGATGCTCCAAGTCATAGAAATGGGAAAAGCAAATGGTCATTCCTGTTCAGTTTG
ACAGACCTGAAATCAATCAAGCAAAACAAAGAGGGTATGGGCTGGTCCTATTTGGTATTC
TGTCTAAAGGATGACGTCGTTCTCCCTGCTCTACACTTTCATCAAGGAGATAGCAAACTA
CTGATTGAATCTCTTGAAAAATATGTGGTATTGTGTGAATCTCCACAGGATAAAAGAACA
CTTCTTGTGAATTGTCAGAATAAGAGTCTTTCACAGTCTTTTGAAAATCTTCTTGATGAG
CCAGCATATGGTTTAATACAAAAAATTAAAAAGGACCCTTATACGGCAACTATGATAGGA
TTTTCCAAAGTCACAAACTACATTTTTGACAGTTTGAGAGGCAGCGATCCCTCTACACAT
CAACGACCACCTTCAGAAATGGCAGATTTTCTTAGTGATGCTATTCCAGGTCTAAAGATA
AATCAACAAGAAGAACCAGGATTTGAAGTCATCACAAGAATTGATTTGGGGGAACGCCCT
GTTGTTCAAAGGAGAGAACCGGTATCACTGGAAGAATGGACTAAGAACATTGATTCTGAA
GGAAGAATTTTAAATGTAGATAATATGAAGCAGATGATATTTAGAGGGGGACTTAGTCAT
GCATTGAGAAAGCAAGCATGGAAATTTCTTCTGGGTTATTTTCCCTGGGACAGTACCAAG
GAGGAAAGAACCCAATTACAAAAGCAAAAAACTGATGAATACTTCAGAATGAAACTGCAG
TGGAAATCCATCAGCCAGGAACAAGAGAAAAGAAATTCGAGGTTAAGAGATTATAGAAGT
CTTATCGAAAAAGATGTTAACAGAACAGATCGAACAAACAAGTTTTATGAAGGCCAAGAT
AATCCAGGGTTGATTTTACTTCATGACATTTTGATGACCTACTGTATGTATGATTTTGAT
TTAGGATATGTTCAAGGAATGAGTGATTTACTTTCCCCTCTTTTATATGTGATGGAAAAT
GAAGTGGATGCCTTTTGGTGCTTTGCCTCTTACATGGACCAAATGCATCAGAATTTTGAA
GAACAAATGCAAGGCATGAAGACCCAGCTAATTCAGCTGAGTACCTTACTTCGATTGTTA
GACAGTGGATTTTGCAGTTACTTAGAATCTCAGGACTCTGGATACCTTTATTTTTGCTTC
AGGTGGCTTTTAATCAGATTCAAAAGGGAATTTAGTTTTCTAGATATTCTTCGATTATGG
GAGGTAATGTGGACCGAACTACCATGTACAAATTTCCATCTTCTTCTCTGTTGTGCTATT
CTGGAATCAGAAAAGCAGCAAATAATGGAAAAGCATTATGGCTTCAATGAAATACTTAAG
CATATCAATGAATTGTCCATGAAAATTGATGTGGAAGATATACTCTGCAAGGCAGAAGCA
ATTTCTCTACAGATGGTAAAATGCAAGGAATTGCCACAAGCAGTCTGTGAGATCCTTGGG
CTTCAAGGCAGTGAAGTTACAACACCAGATTCAGACGTTGGTGAAGACGAAAATGTTGTC
ATGACTCCTTGTCCTACATCTGCATTTCAAAGTAATGCCTTGCCTACACTCTCTGCCAGT
GGAGCCAGAAATGACAGCCCAACACAGATACCAGTGTCCTCAGATGTCTGCAGATTAACA
CCTGCA
Restriction Sites Please inquire     
ACCN NM_001146214
ORF Size 2049 bp
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).
OTI Annotation This TrueClone is provided through our Custom Cloning Process that includes sub-cloning into OriGene's pCMV6 vector and full sequencing to provide a non-variant match to the expected reference without frameshifts, and is delivered as lyophilized plasmid DNA.
Reference Data
RefSeq NM_001146214.1, NP_001139686.1
RefSeq Size 5852
RefSeq ORF 2049
Locus ID 64786
Gene Summary This gene encodes a member of the Ras-like proteins in brain-GTPase activating protein superfamily that share a conserved Tre-2/Bub2/Cdc16 domain. The encoded protein interacts with Ras-like protein in brain 5A and may function as a regulator of intracellular trafficking. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]
Transcript Variant: This variant (2) contains an alternate in-frame exon in the 5' coding region and uses a distinct start codon compared to variant 1. The encoded isoform (2) has a distinct and shorter N-terminus compared to isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

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