DIP2A (NM_001146115) Human Untagged Clone

CAT#: SC327649

DIP2A (untagged)-Human DIP2 disco-interacting protein 2 homolog A (Drosophila) (DIP2A) transcript variant 6


  "NM_001146115" in other vectors (4)

Reconstitution Protocol

USD 760.00

5 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol DIP2A
Synonyms C21orf106; DIP2
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>NCBI ORF sequence for NM_001146115, the custom clone sequence may differ by one or more nucleotides
ATGGCTGACCGCGGGTGCCCGCTGGAGGCGGCGCCGCTGCCTGCCGAGGTGCGGGAGAGC
CTGGCTGAGCTGGAGCTGGAGCTGTCGGAAGGTGACATCACTCAAAAAGGATATGAAAAG
AAAAGGGCAAAGCTGCTTGCACGTTATATACCGCTTATTCAAGGAATAGACCCATCTCTG
CAAGCAGAGAATAGAATTCCTGGGCCCTCACAAACCACGGCCGCTGCACCCAAGCAGCAG
AAGTCTCGGCCCACCGCCTCGAGGGATGAGCGCTTCCGGTCAGATGTCCACACTGAAGCC
GTGCAAGCAGCTTTGGCCAAATACAAAGAGAGGAAGATGCCTATGCCTTCGAAGAGACGT
TCTGTCCTTGTGCATTCGTCTGTGGAAACCTACACCCCTCCAGACACGTCGTCTGCCTCA
GAAGATGAGGGCTCTTTACGGCGACCCGGGCGACTCACCTCCACTCCGCTCCAGAGCCAT
TCCAGCGTCGAGCCCTGGCTCGACCGGGTCATTCAGGGCTCGTCCACCTCATCCTCTGCA
TCCTCCACCTCATCTCACCCGGGAGGGAGACCCACCACTGCTCCCAGTGCTGCAGCCACG
CCGGGGGCCGCCGCTACCACTGCACTCGCAGGCCTCGAGGCCCACACCCACATAGGTGTC
CCTGTGAACAGCAGAGTGTCCTCCAAAATCCAGCAGCTTCTGAACACCCTGAAGAGGCCA
AAGCGCCCTCCACTGAAGGAGTTCTTTGTGGATGATTTTGAGGAATTGTTGGAAGTTCAG
CAACCAGATCCAAATCAGCCAAAGCCTGAGGGAAGCGAGACGAGTGTGCTGAGAGGGGAG
CCTCTCACTGCAGGTGTCCCCCGACCGCCGTCGCTGTTGGCCACCTTGCAGCGCTGGGGC
ACAACACAGCCCAAATCCCCCTGTCTGACTGCCTTGGATACAACTGGGAAAGCCGTCTAC
ACTCTCACCTATGGTAAACTTTGGAGTCGGAGTTTAAAACTAGCTTATACTCTACTTAAT
AAACTGACAAGTAAGAATGAACCTCTACTTAAACCTGGAGACAGAGTGGCGCTCGTGTTT
CCGAATAGTGACCCTGTGATGTTCATGGTTGCATTTTATGGGTGTCTCCTGGCAGAGCTG
GTTCCTGTCCCCATAGAAGTGCCATTAACAAGAAAGGATGCAGGCAGCCAGCAGGTTGGG
TTTCTGCTGGGCAGCTGTGGAGTCTTCTTGGCCCTGACCACAGACGCTTGTCAGAAAGGC
CTCCCCAAGGCACAGACAGGAGAGGTGGCAGCTTTCAAAGGTTGGCCCCCGCTCTCCTGG
CTAGTGATTGATGGGAAGCATCTAGCCAAGCCCCCAAAGGACTGGCACCCTCTGGCCCAG
GACACAGGGACTGGGACTGCCTACATTGAGTATAAAACCAGCAAAGAAGGCAGTACGGTG
GGGGTCACAGTGTCCCACGCATCCCTGCTGGCACAGTGCCGGGCTCTGACCCAGGCGTGC
GGGTACTCAGAAGCTGAAACATTAACAAACGTGCTGGATTTCAAAAGGGATGCTGGTCTG
TGGCATGGCGTGTTAACAAGCGTCATGAACAGGATGCACGTGGTCAGCGTCCCCTACGCG
CTGATGAAGGCGAACCCACTCTCCTGGATCCAGAAAGTGTGCTTCTATAAAGCTCGGGCC
GCGCTGGTGAAGTCGCGAGACATGCACTGGTCTCTCCTAGCTCAGCGGGGCCAGAGGGAC
GTCAGCCTCAGCTCACTGCGCATGCTGATTGTGGCCGATGGTGCCAACCCGTGGTCGATC
TCCTCCTGTGACGCCTTCCTCAACGTCTTCCAGTCCAGAGGTCTGAGGCCAGAGGTCATC
TGTCCTTGTGCAAGTTCTCCTGAGGCGCTGACTGTCGCCATCCGCAGGCCACCTGATCTG
GGAGGACCACCTCCAAGAAAAGCAGTCCTGTCGATGAACGGTCTAAGTTATGGTGTTATC
AGAGTGGATACTGAAGAAAAGTTGTCAGTCCTTACTGTTCAGGACGTTGGTCAGGTGATG
CCTGGAGCTAATGTATGTGTTGTGAAGTTAGAAGGTACCCCTTATCTTTGTAAAACTGAT
GAAGTGGGAGAAATATGCGTCAGTTCCAGTGCAACTGGCACAGCGTACTATGGATTGCTT
GGAATCACGAAGAATGTGTTTGAGGCAGTTCCGGTCACCACAGGAGGAGCACCCATCTTT
GACAGGCCATTCACCAGGACAGGCCTGCTGGGCTTCATCGGGCCTGACAACCTGGTCTTC
ATCGTGGGCAAACTGGACGGGCTGATGGTCACTGGAGTTCGCAGACACAATGCAGATGAC
GTTGTGGCCACCGCACTGGCCGTGGAGCCCATGAAGTTTGTCTACAGAGGCAGG
Restriction Sites Please inquire     
ACCN NM_001146115
ORF Size 2397 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_001146115.1, NP_001139587.1
RefSeq Size 2758
RefSeq ORF 2397
Locus ID 23181
Gene Summary The protein encoded by this gene may be involved in axon patterning in the central nervous system. This gene is not highly expressed. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
Transcript Variant: This variant (6) lacks an alternate in-frame exon and differs in the 3' UTR and coding region compared to variant 1, that causes a frameshift. The resulting isoform (f) is shorter and has a distinct C-terminus compared to isoform a.

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