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)
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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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Other Versions
SKU | Description | Size | Price |
---|---|---|---|
RC217264 | SLC44A4 (Myc-DDK-tagged)-Human solute carrier family 44, member 4 (SLC44A4), transcript variant 1 |
USD 610.00 |
|
RG217264 | SLC44A4 (GFP-tagged) - Human solute carrier family 44, member 4 (SLC44A4), transcript variant 1 |
USD 670.00 |
|
RC217264L1 | Lenti-ORF clone of SLC44A4 (Myc-DDK-tagged)-Human solute carrier family 44, member 4 (SLC44A4), transcript variant 1 |
USD 1,008.00 |
|
RC217264L2 | Lenti-ORF clone of SLC44A4 (mGFP-tagged)-Human solute carrier family 44, member 4 (SLC44A4), transcript variant 1 |
USD 810.00 |
|
RC217264L3 | Lenti-ORF clone of SLC44A4 (Myc-DDK-tagged)-Human solute carrier family 44, member 4 (SLC44A4), transcript variant 1 |
USD 810.00 |
|
RC217264L4 | Lenti-ORF clone of SLC44A4 (mGFP-tagged)-Human solute carrier family 44, member 4 (SLC44A4), transcript variant 1 |
USD 1,008.00 |
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