CCDC115 (NM_032357) Human Untagged Clone

CAT#: SC319126

CCDC115 (untagged)-Human coiled-coil domain containing 115 (CCDC115)


  "NM_032357" in other vectors (4)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol CCDC115
Synonyms ccp1; CDG2O
Vector pCMV6-AC
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection Neomycin
Sequence Data
>OriGene sequence for NM_032357.2 CCAGATCTGGAGGTGTGTCCATGGCGGCGCTTGACCTGCGAGCGGAGCTGGATTCGCTGG
TCCTGCAGCTGCTTGGGGACCTGGAGGAGCTGGAGGGGAAACGAACGGTGTTGAACGCCC
GGGTGGAGGAGGGCTGGCTCTCGCTCGCCAAGGCTCGCTACGCGATGGGCGCCAAGTCGG
TAGGGCCCCTGCAGTATGCTTCCCACATGGAGCCCCAGGTCTGCCTCCACGCCAGCGAGG
CCCAGGAGGGACTCCAGAAGTTCAAGGTGGTGAGAGCTGGTGTCCACGCCCCAGAGGAGG
TGGGGCCTCGCGAAGCAGGTCTGCGGAGGCGCAAGGGCCCCACTAAGACCCCAGAACCGG
AGTCCTCTGAGGCCCCTCAGGACCCCCTGAACTGGTTTGGAATCCTAGTTCCTCACAGTC
TACGTCAGGCTCAAGCAAGCTTCCGGGATGGCCTGCAGCTGGCCGCAGACATAGCCAGCC
TCCAGAACCGCATTGACTGGGGTCGAAGCCAGCTCCGGGGACTCCAAGAGAAACTCAAGC
AGCTGGAGCCTGGGGCTGCCTGACATGCGCGCAAAGAGGCAGGGCAGCGAGCACAGCTGT
TCTCCGACATGGCTACGTGATCTCAGGCCTTCTTCCTTCACAATTAGCTCTTGCCCCTAC
CCCACGCCAGCTAATGCCCCTTCTGTGTCCCTGCTCTGCATGTTTCCATTTTCCTTAGGT
GTGAAGTTTGAAGAGGCAAACAGTAATTTTGAAAGCCACTACTTTGAAACCATTCTAAGG
CCTGAGTTCCCATAGGACACACTCACATAGGCAGGTACACGTTAGTCAACAATTGGAACT
GCCTCTTGGATCACTCAGCTGTGCTTTCATGGCTGGATGATGGAACACTGTGCGAAGAGA
GATGGGGGCCAGGAAGTAGCGCTTCATGCTTAGTACATCCTCCAAATTGTCTTTGCTGGA
GGAGAAAACCGTACTCAGCCAAAAGATCAGGACAATATGACTTGAGTCCACAAGGACACA
AACACCTGAGTAGCTGGGCAGCCCTTGGCAGGGTCTAAGCCAGGAAGTAAAAATGATCTG
GCCTAGATATTTAAGGGAACTCTAGGAAGAGGCCTAGGTTTTTAAAATCCTGTCTCTTTG
TCTTACCATAAGAGGCTGAGCCTCTCTTCATTTTTTTGAAGGGCCACTTGTGTTTTCTGT
TCTGGGAACTTCATTCATTTTTCTACTGGGTTGTTGATCTTTGCAGTAATTTCTAGGAGC
TGTTTATGTTTGGAGGTAATTGGTCCTTTGTCCATATATATGAGATGTAAGTCTTATTTT
CCAGTTTATCTTTTTGCTTATTTTTTTTGACTTTTTATTGTAAAATAAAACATCAAACTG
CACAGAACAGTTGAATAGCTTAATGAATAACTACAGTAAAAGCTATGGTAACCACTACCC
AAAAAAAAAAAAAAAAAAAA
>OriGene 5' read for NM_032357.2 unedited
TCATGTGTATACGACTCCTATAGGGCGGCCGGGAATTCGGCACGAGGCCAGATCTGGAGG
TGTGTCCATGGCGGCGCTTGACCTGCGAGCGGAGCTGGATTCGCTGGTCCTGCAGCTGCT
TGGGGACCTGGAGGAGCTGGAGGGGAAACGAACGGTGTTGAACGCCCGGGTGGAGGAGGG
CTGGCTCTCGCTCGCCAAGGCTCGCTACGCGATGGGCGCCAAGTCGGTAGGGCCCCTGCA
GTATGCTTCCCACATGGAGCCCCAGGTCTGCCTCCACGCCAGCGAGGCCCAGGAGGGACT
CCAGAAGTTCAAGGTGGTGAGAGCTGGTGTCCACGCCCCAGAGGAGGTGGGGCCTCGCGA
AGCAGGTCTGCGGAGGCGCAAGGGCCCCACTAAGACCCCAGAACCGGAGTCCTCTGAGGC
CCCTCAGGACCCCCTGAACTGGTTTGGAATCCTAGTTCCTCACAGTCTACGTCAGGCTCA
AGCAAGCTTCCGGGATGGCCTGCAGCTGGCCGCAGACATAGCCAGCCTCCAGAACCGCAT
TGACTGGGGTCGAAGCCAGCTCCGGGGACTCCAAGAGAAACTCAAGCAGCTGGAGCCTGG
GGCTGCCTGACATGCGCGCAAAGAGGCAGGGCAGCGAGCACAGCTGTTCTCCGACATGGC
TACGTGATCTCAGCCTTCTTCCTTCACAATTAGCTCTTGCCCCTACCCCACGCCAGCTAA
TGCCCCTTCTGTGTCCCTGCTCTGCATGTTTCCATTTTCCTTAGTGTGAAGTTTGAGAGG
CAAACAGTAATTTTGAAAGCCACTACTTTGAAACCATCTAAGCCCTGAGTTCCCATAGAC
CACTCACATAGCAGTACACGTTAGTCAACAATGCACTGCTCTGATCACTCAGCTGTGCCT
TTCATGCCTGATGAATGACACTGGTGGCGAAAAAGGAATGGGGGCCCAGAGT
Restriction Sites Please inquire     
ACCN NM_032357
ORF Size 543 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_032357.2, NP_115733.2
RefSeq Size 1644
RefSeq ORF 543
Locus ID 84317
Gene Summary The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans. [provided by RefSeq, Mar 2016]
Transcript Variant: This variant (1) encodes the longest isoform (a). 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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