SPTLC1 (NM_178324) Human 3' UTR Clone

CAT#: SC207104

3`UTR clone of serine palmitoyltransferase long chain base subunit 1 (SPTLC1) transcript variant 2 for miRNA target validation


Reconstitution Protocol

USD 560.00

4 Weeks*

Size
    • 10 ug

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Specifications

Product Data
Vector pMirTarget
Species Human
Transfection Reporter RFP
Assay Reporter Luciferase
E. coli Selection Kanamycin (25 ug/mL)
Mammalian Cell Selection Neomycin
Symbol SPTLC1
Synonyms HSAN1; HSN1; LBC1; LCB1; SPT1; SPTI
ACCN NM_178324
Insert Size 508
Sequence Data
>SC207104 3'UTR clone of NM_178324
The sequence shown below is from the reference sequence of NM_178324. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon


CAATTGGCAGAGCTCAGAATTCAAGCGATCGC

ACTTGTGGACCCAGAGGATTTTATGGCACATTTGAATGAAGATGAAGGATCATTGATTTCCTTGTGTATG
GATAATCCGGGAACAGGCCAACTAAATATTTGATGAATGTATGATTTCAAATACAGTGAATTCCCTGGGA
GTCATCAAAGAAGACCGGCATTTTATGGTTGTTTTTATTAAGTGTATATTCTTTGCTCCTGAAAATGTTA
TTAAATAATTGTTTAGGCCGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTCAAAGGCTGAGGCAG
GCAGATCACCTGAGGTCAGGAGTTCAAAACCAGCCTGGCCAACATGCTGAAACCTCGTCTCTACTAAAAA
TACAAAAATTAGCTGGGCGTGGTGGTGGATACCTGTAATCCCAGCTACGTGGGAGGCTGAGGTGGGAGAA
TTGCTTCAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGCAACA
GAGCAAGACTGTCTCAAA

ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG
Restriction Sites SgfI-MluI     
OTI Disclaimer Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq NM_178324.1
Summary This gene encodes a member of the class-II pyridoxal-phosphate-dependent aminotransferase family. The encoded protein is the long chain base subunit 1 of serine palmitoyltransferase. Serine palmitoyltransferase converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate and is the key enzyme in sphingolipid biosynthesis. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified. Pseudogenes of this gene have been defined on chromosomes 1, 6, 10, and 13. [provided by RefSeq, Jul 2013]
Locus ID 10558

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