PNPLA8 (NM_001256011) Human Untagged Clone
CAT#: SC330349
PNPLA8 (untagged) - Homo sapiens patatin-like phospholipase domain containing 8 (PNPLA8), transcript variant 6
"NM_001256011" in other vectors (2)
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | PNPLA8 |
Synonyms | IPLA2-2; IPLA2G; iPLA2gamma; MMLA; PNPLA-gamma |
Vector | pCMV6 series |
Sequence Data |
>NCBI ORF sequence for NM_001256011, the custom clone sequence may differ by one or more nucleotides
ATGTCCCGTATTAAAAGTACTTTGAACTCTGTTTCAAAGGCTGTTTTTGGCAATCAAAATGAAATGATTT CACGTTTAGCTCAATTTAAGCCAAGTTCCCAAATTTTAAGAAAAGTATCGGATAGTGGCTGGTTAAAACA GAAAAACATCAAACAAGCCATCAAATCTCTGAAAAAATATAGTGACAAATCAGCAGAAAAGAGTCCTTTT CCAGAAGAGAAAAGTCACATTATAGACAAAGAAGAAGATATAGGTAAACGCAGTCTTTTTCATTACACAA GTTCTATAACCACAAAATTTGGAGACTCATTCTACTTTTTATCAAATCATATTAATTCATATTTCAAACG TAAGGAAAAAATGTCTCAACAAAAGGAAAATGAACATTTCCGGGACAAATCAGAACTTGAAGATAAAAAG GTAGAAGAGGGGAAATTAAGATCTCCAGATCCTGGCATCCTGGCTTATAAGCCAGGCTCAGAATCTGTAC ATACGGTGGACAAGCCTACAAGTCCTTCTGCGATACCTGATGTTCTTCAAGTTTCAACTAAACAAAGTAT TGCTAACTTTCTTTCTCGTCCCACGGAAGGTGTACAAGCTTTAGTAGGTGGTTATATTGGTGGACTTGTC CCCAAATTAAAGTATGATTCAAAGAGTCAGTCAGAAGAACAGGAAGAGCCTGCTAAAACTGATCAGGCTG TCAGCAAAGACAGAAATGCAGAGGAGAAAAAGCGTTTATCTCTTCAGCGAGAAAAGATTATCGCAAGGGT GAGTATTGATAACAGGACCCGGGCATTAGTTCAGGCATTAAGAAGAACAACTGACCCAAAGCTCTGCATT ACTAGGGTTGAAGAACTGACTTTTCATCTTCTAGAATTTCCTGAAGGAAAAGGAGTGGCTGTCAAGGAAA GAATTATTCCATATTTATTACGACTGAGACAAATTAAGGATGAAACTCTTCAGGCTGCAGTTAGAGAAAT TTTGGCCCTAATTGGCTATGTGGATCCAGTGAAAGGGAGAGGAATCCGAATTCTCTCAATTGATGGTGGA GGAACAAGGGGCGTGGTTGCTCTCCAGACCCTACGAAAATTAGTTGAACTTACTCAGAAGCCAGTTCATC AGCTCTTTGATTACATTTGTGGTGTAAGCACAGGTGCCATATTAGCTTTCATGTTGGGGTTGTTTCATAT GCCCTTGGATGAATGTGAGGAACTTTATCGAAAATTAGGATCAGATGTATTTTCACAAAATGTCATTGTT GGAACAGTAAAAATGAGTTGGAGCCATGCATTTTATGACAGTCAAACATGGGAAAACATTCTTAAGGATA GGATGGGATCTGCACTGATGATTGAAACAGCAAGAAACCCCACATGTCCTAAGGTAGCTGCTGTAAGTAC CATAGTAAATAGAGGGATAACACCCAAAGCTTTTGTGTTCAGAAACTATGGTCATTTTCCTGGAATCAAC TCTCATTATTTGGGAGGCTGTCAGTATAAAATGTGGCAGGCCATTAGAGCCTCATCTGCTGCTCCAGGCT ACTTTGCAGAATATGCATTGGGAAATGATCTTCATCAAGATGGAGGTTTGCTTCTGAATAACCCTTCGGC ATTAGCTATGCATGAGTGTAAATGTCTTTGGCCAGATGTGCCGTTAGAGTGCATAGTATCCCTGGGCACT GGACGTTATGAGAGTGATGTGAGAAACACGGTAACATACACAAGCTTGAAAACTAAACTTTCTAATGTTA TCAACAGTGCTACAGATACAGAAGAAGTCCATATAATGCTTGATGGCCTGTTACCTCCTGACACCTATTT TAGATTCAATCCTGTAATGTGTGAAAACATACCTCTAGATGAAAGTCGAAATGAAAAGCTGGATCAGCTG CAGTTGGAAGGGTTGAAATACATAGAAAGAAATGAACAAAAAATGAAAAAAGTTGCAAAAATATTAAGTC AAGAAAAAACAACTCTGCAGAAAATTAATGATTGGATAAAATTAAAAACTGATATGTATGAAGGACTTCC ATTCTTTTCAAAATTGTGA |
Restriction Sites | SgfI-MluI |
ACCN | NM_001256011 |
ORF Size | 2049 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). |
Reference Data | |
RefSeq | NM_001256011.1, NP_001242940.1 |
RefSeq Size | 4435 |
RefSeq ORF | 2049 |
Locus ID | 50640 |
Gene Summary | This gene encodes a member of the patatin-like phospholipase domain containing protein family. Members of this family are phospholipases which catalyze the cleavage of fatty acids from membrane phospholipids. The product of this gene is a calcium-independent phospholipase. Mutations in this gene have been associated with mitochondrial myopathy with lactic acidosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2015] Transcript Variant: This variant (6) differs in the 5' UTR and coding region and uses a downstream start codon compared to variant 1. The resulting protein (isoform 3) has a shorter N-terminus compared to isoform 1. Variants 5 and 6 encode the same protein. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments. |
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