SLC44A4 (NM_025257) Human Untagged Clone

CAT#: SC126791

SLC44A4 (untagged)-Human solute carrier family 44, member 4 (SLC44A4), transcript variant 1


  "NM_025257" in other vectors (6)

Reconstitution Protocol

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol SLC44A4
Synonyms C6orf29; CTL4; DFNA72; hTPPT1; NG22; TPPT
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC126791 sequence for NM_025257 edited (data generated by NextGen Sequencing)
ATGGGGGGAAAGCAGCTGGACGAGGATGACGAGGCCTACGGGAAGCCAGTCAAATACGAC
CCCTCCTTTCGAGGCCCCATCAAGAACAGAAGCTGCACAGATGTCATCTGCTGCGTCCTC
TTCCTGCTCTTCATTCTAGGTTACATCGTGGTGGGGATTGTGGCCTGGTTGTATGGAGAC
CCCCGGCAAGTCCTCTACCCCAGGAACTCTACTGGGGCCTACTGTGGCATGGGGGAGAAC
AAAGATAAGCCGTATCTCCTGTACTTCAACATCTTCAGCTGCATCCTGTCCAGCAACATC
ATCTCAGTTGCTGAGAACGGCCTACAGTGCCCCACACCCCAGGTGTGTGTGTCCTCCTGC
CCGGAGGACCCATGGACTGTGGGAAAAAACGAGTTCTCACAGACTGTTGGGGAAGTCTTC
TATACAAAAAACAGGAACTTTTGTCTGCCAGGGGTACCCTGGAATATGACGGTGATCACA
AGCCTGCAACAGGAACTCTGCCCCAGTTTCCTCCTCCCCTCTGCTCCAGCTCTGGGGCGC
TGCTTTCCATGGACCAACGTTACTCCACCGGCGCTCCCAGGGATCACCAATGACACCACC
ATACAGCAGGGGATCAGCGGTCTTATTGACAGCCTCAATGCCCGAGACATCAGTGTTAAG
ATCTTTGAAGATTTTGCCCAGTCCTGGTATTGGATTCTTGTTGCCCTGGGGGTGGCTCTG
GTCTTGAGCCTACTGTTTATCTTGCTTCTGCGCCTGGTGGCTGGGCCCCTGGTGCTGGTG
CTGATCCTGGGAGTGCTGGGCGTGCTGGCATACGGCATCTACTACTGCTGGGAGGAGTAC
CGAGTGCTGCGGGACAAGGGCGCCTCCATCTCCCAGCTGGGTTTCACCACCAACCTCAGT
GCCTACCAGAGCGTGCAGGAGACCTGGCTGGCCGCCCTGATCGTGTTGGCGGTGCTTGAA
GCCATCCTGCTGCTGATGCTCATCTTCCTGCGGCAGCGGATTCGTATTGCCATCGCCCTC
CTGAAGGAGGCCAGCAAGGCTGTGGGACAGATGATGTCTACCATGTTCTACCCACTGGTC
ACCTTTGTCCTCCTCCTCATCTGCATTGCCTACTGGGCCATGACTGCTCTGTACCTGGCT
ACATCGGGGCAACCCCAGTATGTGCTCTGGGCATCCAACATCAGCTCCTCCGGCTGTGAG
AAAGTGCCAATAAATACATCATGCAACCCCACGGCCCACCTTGTGAACTCCTCGTGCCCA
GGGCTGATGTGCGTCTTCCAGGGCTACTCATCCAAAGGCCTAATCCAACGTTCTGTCTTC
AATCTGCAAATCTATGGGGTCCTGGGGCTCTTCTGGACCCTTAACTGGGTACTGGCCCTG
GGCCAATGCGTCCTCGCTGGAGCCTTTGCCTCCTTCTACTGGGCCTTCCACAAGCCCCAG
GACATCCCTACCTTCCCCTTAATCTCTGCCTTCATCCGCACACTCCGTTACCACACTGGG
TCATTGGCATTTGGAGCCCTCATCCTGACCCTTGTGCAGATAGCCCGGGTCATCTTGGAG
TATATTGACCACAAGCTCAGAGGAGTGCAGAACCCTGTAGCCCGCTGCATCATGTGCTGT
TTCAAGTGCTGCCTCTGGTGTCTGGAAAAATTTATCAAGTTCCTAAACCGCAATGCATAC
ATCATGATCGCCATCTACGGGAAGAATTTCTGTGTCTCAGCCAAAAATGCGTTCATGCTA
CTCATGCGAAACATTGTCAGGGTGGTCGTCCTGGACAAAGTCACAGACCTGCTGCTGTTC
TTTGGGAAGCTGCTGGTGGTCGGAGGCGTGGGGGTCCTGTCCTTCTTTTTTTTCTCCGGT
CGCATCCCGGGGCTGGGTAAAGACTTTAAGAGCCCCCACCTCAACTATTACTGGCTGCCC
ATCATGACCTCCATCCTGGGGGCCTATGTCATCGCCAGCGGCTTCTTCAGCGTTTTCGGC
ATGTGTGTGGACACGCTCTTCCTCTGCTTCCTGGAAGACCTGGAGCGGAACAACGGCTCC
CTGGACCGGCCCTACTACATGTCCAAGAGCCTTCTAAAGATTCTGGGCAAGAAGAACGAG
GCGCCCCCGGACAACAAGAAGAGGAAGAAGTGA

Clone variation with respect to NM_025257.2
17 g=>t;1189 c=>t
>OriGene 5' read for NM_025257 unedited
TGTAATACGACTCACTATAGGGCGGCCGCGAATTCGGCACGAGGGCCATGGGGGNGAAAG
CAGCTGGACGAGGATGACGAGGCCTACGGGAAGCCAGTCAAATACGACCCCTCCTTTCGA
GGCCCCATCAAGAACAGAAGCTGCACAGATGTCATCTGCTGCGTCCTCTTCCTGCTCTTC
ATTCTAGGTTACATCGTGGTGGGGATTGTGGCCTGGTTGTATGGAGACCCCCCGCAAGTC
CTCTACCCCAGGAACTTTACTGGGGCCTTACTGGGGCAGGGGGGAAAAACAAAAAAAAAC
CCGTTTTTTCCGGGGTTTTCAAAATTTTTAAGGGGGGGGCCGGGGCCCAAAAAAATTTTT
TTTTTTTTTTAGTAAAAAAGAGGTTTTATGCCCCCCCCCCCCCCAGGTGGGGGGGTGTTT
TTCTTTCCCCCGGGGGAGAAAAATTTTTGTGTGGTTAAAAAAAAAAACAACCCCCCCCCC
CGCGCGGGGGGGGGGGGTTTTTTTATAAAAAAAAAAAATATTTTTTTTTTTTTTGCGGCG
GCCCGCCCCTTAATTTAAATAAAAAAAAAAACCCCCCCCCGAAGCCGGGGNNNNTTGGTT
TTTCTCCCTCCCCCCCCCCCCTTTTGGTGGGGGGGGGGGGGGGGTGTTAAAAAAAAAAAC
AAACACCCCCCCCCCCCGCGCGGGGCCGGGNGGGTGCACCCCCCCCCACCCCCTCGGGGG
GGGGGGGGGTTGTTTTTTTTTTCTTTCCCCTCCCCCCCCCCCNCCNNCNCCCAAAACAGC
ATAATATATTTTTTTTTNCTTCTCTCCCCTCCTCCCCTCTCGGCGGGCTCCCTGGGGGCG
GGGGGGGGGGGGGGATCTTGGAATTACCATCTCTTCTCCGGTTTCTCCGCCGGGG
>OriGene 3' read for NM_025257 unedited
TGGACCGCGGCCGCAATCTANAGTCGAGTTTTTTTTTTTTTTTTTTTTGAGTTAACAAAA
TATCTTTAATAAAATCTTTTTGTTTGTTTGTTTTGTTTTGGAGACAGAGTCTGTCACCCA
GGTTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCG
ATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATGACAGGTGCATGCCACCATTCTCGGC
TAATTTTTGTATTTTTAATAGAGACGGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAA
CTCCTGACTCAGGTGATCCGCCCGCCTCAGCCTCTCAAAGTGTTGGATTACAGGCGTGAG
CCACGGCGCCTGGCCTAAAACCTTTTTTTACCACAAAATGGAGACCTGTAAGGCGAAGTG
AGGTTGGATGGCTGGACGGTGGGGGTGGGGTGCAGTCCTGGATCAGGGCCGGAGCTGTCA
CTTCTTCCTCTTCTTGTTGTCCGGGGGCGCCTCGTTCTTCTTGCCCAGAATCTTTAGAAG
GCTCTTGGACATGTAGTAGGGCCGGTCCAGGGAGCCGTTGTTCCGCTCCAAGTCTTCCAG
GAAGCAGAGGAAGAGCGTGTCCACACACATGCCGAAAACCCTGAAGAAGCCGCTGGCGAT
GACATATGCCCCCAGGATGGATGTCATGATGGGCACCCAGTAATAGTTGAGGTGGGGGCT
CTTAAATCTTTCCCCCACCCCCGGATGCCACCGGAGAAAAAAAGAAGGACAGGACCCCCC
CCCTCCAACCACAACAGTTTCCCAAAGACAGCAGCAGTCTTGGACTTTGCCCAGACGACC
CCCCGCCATGTCCCCCTGATTAGCTGACCCCTTTTTGGCCTACCCCAAAAATCTCCCCCG
AAATGGCACCTGAGCCTCCCTGCGGCCAGAACTGATAAATTTTCCAACCTAAGCCACCTG
Restriction Sites NotI-NotI     
ACCN NM_025257
ORF Size 2139 bp
Insert Size 2620
OTI Disclaimer Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery.

The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
Reference Data
RefSeq NM_025257.1, NP_079533.1
RefSeq Size 2347
RefSeq ORF 2139
Locus ID 80736
Domains DUF580
Protein Families Transmembrane
Gene Summary The protein encoded by this gene may be a sodium-dependent transmembrane transport protein involved in the uptake of choline by cholinergic neurons. Defects in this gene can cause sialidosis, a lysosomal storage disease. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2010]
Transcript Variant: This variant (1) encodes the longest isoform (1).

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