MAGEA12 (NM_005367) Human Untagged Clone

CAT#: SC122712

MAGEA12 (untagged)-Human melanoma antigen family A, 12 (MAGEA12), transcript variant 3


  "NM_005367" in other vectors (4)

Reconstitution Protocol

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    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol MAGEA12
Synonyms CT1.12; MAGE12
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene sequence for NM_005367 edited
GATTCTCGCCCTGAGCAACGGCCTGACGTCGGTGGAGGGAAGCAGGCGCAGGCTCCGTGA
GGAGGCAAGGTTCTGAGGAGACAGGCCCCGGAGCAGCACTAGCTCCTGCCCACACTCCTA
CCTGCTGCCCTGACCAGAGTCATCATGCCACTTGAGCAGAGGAGTCAGCACTGCAAGCCT
GAGGAAGGCCTTGAGGCCCAAGGAGAGGCCCTGGGCTTGGTGGGTGCGCAGGCTCCTGCT
ACTGAGGAGCAGGAGACTGCCTCCTCCTCCTCTACTCTAGTGGAAGTCACCCTGCGGGAG
GTGCCTGCTGCCGAGTCACCAAGTCCTCCCCACAGTCCTCAGGGAGCCTCCACCCTCCCC
ACTACCATCAACTATACTCTCTGGAGTCAATCCGATGAGGGCTCCAGCAACGAAGAACAG
GAAGGGCCAAGCACCTTTCCTGACCTGGAGACGAGCTTCCAAGTAGCACTCAGTAGGAAG
ATGGCTGAGTTGGTTCATTTTCTGCTCCTCAAGTATCGAGCCAGGGAGCCATTCACAAAG
GCAGAAATGCTGGGGAGTGTCATCAGAAATTTCCAGGACTTCTTTCCTGTGATCTTCAGC
AAAGCCTCCGAGTACTTGCAGCTGGTCTTTGGCATCGAGGTGGTGGAAGTGGTCCGCATC
GGCCACTTGTACATCCTTGTCACCTGCCTGGGCCTCTCCTACGATGGCCTGCTGGGCGAC
AATCAGATCGTGCCCAAGACAGGCCTCCTGATAATCGTCCTGGCCATAATCGCAAAAGAG
GGCGACTGTGCCCCTGAGGAGAAAATCTGGGAGGAGCTGAGTGTGTTGGAGGCATCTGAT
GGGAGGGAGGACAGTGTCTTTGCGCATCCCAGGAAGCTGCTCACCCAAGATTTGGTGCAG
GAAAACTACCTGGAGTACCGGCAGGTCCCCGGCAGTGATCCTGCATGCTACGAGTTCCTG
TGGGGTCCAAGGGCCCTCGTTGAAACCAGCTATGTGAAAGTCCTGCACCATTTGCTAAAG
ATCAGTGGAGGACCTCACATTTCCTACCCACCCCTGCATGAATGGGCTTTTAGAGAGGGG
GAAGAGTGAGTCTGAGCACGAGTTGCAGCCAGGGCCAGTGGGAGGGGGTCTGGGCCAGTG
CACCTTCCAAGGCCCCATCCATTAGTTTCCACTGCCTCGTGTGACATGAGGCCCATTCTT
CACTCTTTGAAGAGAGCAGTCAGTATTGTTAGTAGTGAGTTTCTGTTCTATTGGATGACT
TTGAGATTTATCTTTGTTTCCTGTTGGAATTGTTCAAATGTTCCTTTTAACGGATGGTTG
AATGAACTTCAGCATCCAAGTTTATGAATGACAGTAGTCACACATAGTGCTGTTTATATA
GTTTAGGAGTAAGAGTGTTGTTTTTTATTCAGATTGGGAAATCCATTCCATTTTGTGAAT
TGTGACAAATAACAGCAGTGGAAAAAGTATGTGCTTAGAATTGTGAAAGAATTAGCAGTA
AAATACATGAGATAAAGACCTCAAGAAGTTAAAAGATACTTAATTCTTGCCTTATACCTC
ACTCTATTCTGTAAATTTGAAAAAAAAGCATGGATACCTGGATATCCTTGGCTTCTTTGA
GAATTTAAGAGAAATTAAATCTGAATAAATAAAAAAAAAAAAAAAA
>OriGene 5' read for NM_005367 unedited
NNNGGGGGTTCGGTTTTGTATACGACTCATATAGGGCGGCCGCGATTCCCGGGATATCGT
CGACCCAGCGTCCGCCCACGCGTCCGGATTCTCGCCCTGAGCAACGGCCTGACGTCGGTG
GAGGGAAGCAGGCGCAGGCTCCGTGAGGAGGCAAGGTTCTGAGGAGACAGGCCCCGGAGC
AGCACTAGCTCCTGCCCACACTCCTACCTGCTGCCCTGACCAGAGTCATCATGCCACTTG
AGCAGAGGAGTCAGCACTGCAAGCCTGAGGAAGGCCTTGAGGCCCAAGGAGAGGCCCTGG
GCTTGGTGGGTGCGCAGGCTCCTGCTACTGAGGAGCAGGAGACTGCCTCCTCCTCCTCTA
CTCTAGTGGAAGTCACCCTGCGGGAGGTGCCTGCTGCCGAGTCACCAAGTCCTCCCCACA
GTCCTCAGGGAGCCTCCACCCTCCCCACTACCATCAACTATACTCTCTGGAGTCAATCCG
ATGAGGGCTCCAGCAACGAAGAACAGGAAGGGCCAAGCACCTTTCCTGACCTGGAGACGA
GCTTCCAAGTAGCACTCAGTAGGAAGATGGCTGAGTTGGTTCATTTTCTGCTCCTCAAGT
ATCGAGCCAGGGAGCCATTCACAAAGGCAGAAATGCTGGGGAGTGTCATCAGAAATTTCC
AGGACTTCTTTCCTGTGATCTTCAGCAAAGCCTCCGAGTACTTGCAGCTGGTCTTTGGCA
TCGAGGTGGTGGAAGTGGTCCGCATCGGCCACTTGTACATCCTTGTCACCTGCCTGGGCC
TCTCCTACGATGGCCTGCTGGGCGACAATCAGATCGTGCCCAAGACAGGCCTCCTGATAA
TCGTCCCTGCCATAATCGCAAAAGAGGGCGACTGTGCA
Restriction Sites Please inquire     
ACCN NM_005367
ORF Size 945 bp
Insert Size 1678
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_005367.4, NP_005358.2
RefSeq Size 1666
RefSeq ORF 945
Locus ID 4111
Gene Summary This gene is closely related to several other genes clustered on chromosome X. These genes may be overexpressed in tumors. Multiple alternatively spliced variants encoding the same protein have been identified. [provided by RefSeq, Jun 2014]
Transcript Variant: This variant (3) differs in the 5' UTR compared to variant 1. Variants 1, 2 and 3 all encode the same protein. 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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