VPS13B (NM_015243) Human Untagged Clone

CAT#: SC309712

VPS13B (untagged)-Human vacuolar protein sorting 13 homolog B (yeast) (VPS13B), transcript variant 3


  "NM_015243" in other vectors (4)

Reconstitution Protocol

USD 1,760.00

5 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol VPS13B
Synonyms CHS1; COH1
Vector pCMV6 series
Sequence Data
>NCBI ORF sequence for NM_015243, the custom clone sequence may differ by one or more nucleotides
ATGCTGGAGTCATATGTAACTCCAATTTTAATGAGCTATGTGAATCGCTACATCAAGAAC
TTAAAGCCGTCGGATCTACAGCTTTCACTATGGGGTGGAGACGTGGTACTCAGCAAGCTC
GAGTTAAAGTTGGATGTGCTGGAACAGGAACTGAAATTACCATTCACTTTTTTAAGTGGA
CATATTCATGAATTGAGGATTCATGTACCATGGACAAAACTGGGTTCAGAACCAGTGGTA
ATTACCATCAATACTATGGAATGCATTTTGAAACTTAAGGATGGGATACAGGATGACCAT
GAAAGCTGTGGTTCTAATTCTACCAACCGTAGTACTGCTGAGAGCACAAAATCATCAATC
AAACCGCGGAGAATGCAGCAGGCTGCTCCTACAGATCCTGACTTACCACCAGGTTATGTG
CAGAGTCTGATTAGACGAGTTGTAAATAATGTAAACATTGTGATAAATAATCTCATACTA
AAATATGTTGAAGATGATATCGTCCTTTCCGTCAATATCACTTCTGCAGAATGTTATACA
GTAGGTGAATTATGGGATCGTGCATTCATGGATATTTCTGCAACTGATTTGGTGCTGAGA
AAGGTTATCAATTTTTCTGACTGTACAGTTTGTCTTGATAAACGGAATGCCAGTGGTAAA
ATAGAATTTTACCAGGATCCTTTATTATACAAATGTTCCTTCAGAACTCGTCTTCATTTT
ACATATGAAAACCTAAATTCCAAGATGCCATCTGTTATTAAAATTCATACTTTAGTGGAA
AGTTTGAAACTTTCTATCACAGATCAACAACTGCCTATGTTTATTCGTATAATGCAACTT
GGAATTGCTCTTTACTATGGAGAAATAGGCAATTTTAAAGAAGGCGAAATAGAGGACCTT
ACTTGTCATAATAAAGATATGCTAGGAAACATTACAGGTTCTGAAGATGAAACAAGAATA
GATATGCAATATCCTGCTCAGCATAAAGGTCAAGAGTTATATTCACAGCAAGATGAGGAG
CAGCCACAGGGATGGGTGTCATGGGCCTGGTCCTTTGTGCCTGCAATTGTGAGTTATGAC
GATGGCGAGGAAGACTTTGTTGGGAACGATCCTGCATCAACCATGCATCAACAAAAAGCA
CAGACTTTGAAGGATCCTATTGTTTCTATAGGATTTTATTGCACAAAGGCAACGGTGACT
TTCAAACTCACAGAAATGCAAGTTGAGAGTAGTTATTACAGTCCACAGAAAGTAAAATCT
AAAGAAGTATTGTGTTGGGAACAAGAAGGAACTACAGTTGAGGCCCTTATGATGGGAGAA
CCTTTCTTTGATTGCCAGATTGGGTTTGTTGGTTGCAGAGCCATGTGCCTTAAAGGAATT
ATGGGTGTTAAAGATTTTGAAGAGAATATGAATAGAAGTGAAACTGAAGCCTGTTTCTTC
ATTTGTGGTGACAATTTGAGTACGAAAGGTTTCACATACCTTACAAATTCATTGTTTGAT
TACCGAAGCCCAGAAAATAATGGTACTCGCGCAGAATTTATCTTGGATTCAACTCATCAT
AAGGAGACATACACTGAGATAGCTGGAATGCAACGGTTTGGGGCTTTTTATATGGATTAC
CTGTATACAATGGAGAACACTAGTGGCAAAGGTTCCACAAATCAACAAGACTTTTCTTCA
GGGAAAAGTGAAGATTTGGGAACAGTTCAGGAGAAGTCCACCAAAAGCCTTGTTATAGGT
CCTCTTGATTTTCGTTTGGATAGCAGTGCGGTGCATAGGATTTTGAAAATGATTGTGTGT
GCCTTGGAACATGAATATGAACCATATAGCAGGCTAAAATCAGATATTAAGGATGAAAAT
GAAACAATACTGAATCCTGAAGAGGTGGCTCTTCTGGAGGAATATATTCCTACTCGACAT
ACAAGTGTTACTCTCCTCAAATGTACCTGCACAATTTCCATGGCTGAATTCAACTTGCTG
GACCATTTACTACCTGTCATTATGGGAGAAAAGAACTCAAGTAACTTCATGAATACTACA
AACTTCCAGTCTCTTCGGCCTTTGCCATCCATTCGAATATTGGTGGATAAAATTAATCTG
GAACATTCAGTGCCAATGTATGCTGAACAGTTGGTGCATGTGGTCAGCAGCCTTACTCAA
CCTTCTGATAACCTGCTTCATTATTGTTATGTACACTGCTATCTTAAGATATTTGGTTTC
CAGGCAGGACTGACGTCTTTGGATTGCAGTGGATCTTACTGCTTACCTGTACCAGTTATT
CCCTCTTTCAGCACTGCTCTTTATGGGAAACTTCTGAAACTCCCCACATGCTGGACCAAA
AGATCTCAGATTGCTATAACTGAAGGTATATTTGAACTTCCAAATCTCACAATTCAAGCT
ACAAGAGCACAGACACTTCTCTTGCAAGCAATATATCAAAGTTGGTCTCATCTTGGAAAT
GTCAGCTCTTCCGCAGTGATTGAAGCTTTGATAAATGAAATCTTCCTAAGTATAGAGATT
GGGTCTTGCTATGTTGCCCAGGTTGATCTTGAACTCCTGGCCTCAAATGATCCTCCCACC
TCAACCTCCTGA
Restriction Sites Please inquire     
ACCN NM_015243
ORF Size 2592 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_015243.2, NP_056058.2
RefSeq Size 2822
RefSeq ORF 2592
Locus ID 157680
Gene Summary This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]
Transcript Variant: This variant (3) includes an alternate exon, which results in an early stop codon, compared to variant 5. The resulting isoform (3) has a shorter and distinct C-terminus, compared to isoform 5. 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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*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.