PAF Receptor (PTAFR) (NM_000952) Human Untagged Clone

CAT#: SC119557

PTAFR (untagged)-Human platelet-activating factor receptor (PTAFR), transcript variant 3


  "NM_000952" in other vectors (7)

Reconstitution Protocol

USD 310.00

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Size
    • 10 ug

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Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PTAFR
Synonyms PAFR
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC119557 sequence for NM_000952 edited (data generated by NextGen Sequencing)
ATGGAGCCACATGACTCCTCCCACATGGACTCTGAGTTCCGATACACTCTCTTCCCGATT
GTTTACAGCATCATCTTTGTGCTCGGGGTCATTGCTAATGGCTACGTGCTGTGGGTCTTT
GCCCGCCTGTACCCTTGCAAGAAATTCAATGAGATAAAGATCTTCATGGTGAACCTCACC
ATGGCGGACATGCTCTTCTTGATCACCCTGCCACTTTGGATTGTCTACTACCAAAACCAG
GGCAACTGGATACTCCCCAAATTCCTGTGCAACGTGGCTGGCTGCCTTTTCTTCATCAAC
ACCTACTGCTCTGTGGCCTTCCTGGGCGTCATCACTTATAACCGCTTCCAGGCAGTAACT
CGGCCCATCAAGACTGCTCAGGCCAACACCCGCAAGCGTGGCATCTCTTTGTCCTTGGTC
ATCTGGGTGGCCATTGTGGGAGCTGCATCCTACTTCCTCATCCTGGACTCCACCAACACA
GTGCCCGACAGTGCTGGCTCAGGCAACGTCACTCGCTGCTTTGAGCATTACGAGAAGGGC
AGCGTGCCAGTCCTCATCATCCACATCTTCATCGTGTTCAGCTTCTTCCTGGTCTTCCTC
ATCATCCTCTTCTGCAACCTGGTCATCATCCGTACCTTGCTCATGCAGCCGGTGCAGCAG
CAGCGCAACGCTGAAGTCAAGCGCCGGGCGCTGTGGATGGTGTGCACGGTCTTGGCGGTG
TTCATCATCTGCTTCGTGCCCCACCACGTGGTGCAGCTGCCCTGGACCCTTGCTGAGCTG
GGCTTCCAGGACAGCAAATTCCACCAGGCCATTAATGATGCACATCAGGTCACCCTCTGC
CTCCTTAGCACCAACTGTGTCTTAGACCCTGTTATCTACTGTTTCCTCACCAAGAAGTTC
CGCAAGCACCTCACCGAAAAGTTCTACAGCATGCGCAGTAGCCGGAAATGCTCCCGGGCC
ACCACGGATACGGTCACTGAAGTGGTTGTGCCATTCAACCAGATCCCTGGCAATTCCCTC
AAAAATTAG

Clone variation with respect to NM_000952.4
>OriGene 5' read for NM_000952 unedited
AGGTAAGGCACCCTGCACCCCGCTTGTACTATNAGGGCGGCCGCGCAATTCGCACCAGCA
GNACCCATTCGTAGCCACACGGTCACTGCAGCTGAAGCCGCTGCCCCTGCTACAGGCACC
ACCAGGACCAGCTGATCATTCCAGCCCACAGCAATGGAGCCACATGCCTCCTCCCACAGG
ACTCTGAGTTCCGATACACTCTCTTCCCGACTGTTTACAGCATCATCTTTGTGCTCGGGG
TCATTGCTAATGGCTACGTGCTGTGGGTCTTTGCCCGCCTGTACCCTTGCAAGAAATTCA
ATGAGATAAAGATCTTCATGGCGAACCTCACCATGGCGGACATGCTCTTCTTGATCACCC
TGCCACTTTGGATTGTCTACTACCAAAACCAGGGCAACTGGATACTCCCCAAATTCCTGT
GCAACGTGGCTGGCTGCCTTTTCTTCATCAACACCTACTGCTCTGTGGCCTTCCTGGGCG
TCATCACTTATAACCGCTTCCAGGCAGTAACTCGGCCCATCAAGACTGCTCAGGCCAACA
CCCGCAAGCGTGGCATCTCTTTGTCCTTGGTCATCTGGGTGGCCATTGTGGGAGCTGCAT
CCTACTTCCTCATCCTGGACTCCACCAACACAGTGCCCGACAGTGCTGGCTCAGGCCACG
TCACTCGCTGCTTTGAGCATTACGAGAAGGGCAGCGTGCCAGTCCTCATCATCCACATCT
TCATCGTGGTCAGCTTCTTCCTGGGCCTTCTCATCATCCTCTTTTGCAACCTGGTCATCA
TCCGTACCTTGCTCATGCAGCCGGTGCACCAGCAGCGCACCGCTTAAGTTCAGCGCCCGG
GCGCTGTGGAATGGGTGCCCGTGCTTGGGCGGGGTTCATAATTGCTTCGTGGCCCACCAC
GGGGGGCAGTGCCCTGGACCCTTGTTGACCTGAGCTTCCAGGAACGCG
>OriGene 3' read for NM_000952 unedited
GTCTTGGCCGCGGCCGCATCTANAGTCGGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGA
GATGGAATCTCGCTCTGTTGCCAGGCTAGAGTGCAATGGTGCAATCTAGGTTCACTGCAA
CCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTAC
AGGCGTGTGCCACCATGCCCGGCTAATTTTTGTATGTTTTAGTAGAGATGGGGTTTTACA
ATGTTGGCCAGGATGGTCTCGATCTCTTGACCCATGATCTGCCCACCTCGGCCTCCCAAA
GTGCTGGGATTACAGGTGTGAGCCACTGCGCCCACTCCCCCAAAGCTTTAGACCGATGCC
CCATCGGGGAGAACTAGGTGGTTTAAAGTCTTCCCCCAAGGTCTGCACCTGGCCCTGACA
TTCCTTCCGGCCCCATAAGATTAAGGGACTCAGGATAAAGTCATCAGTCACAGTTACTGT
AGTATGCGCCCACAGGCGGATGAAGGGGCTCATTTGAGTTCTGGATTTTCCAACAGCCTG
GCTCTGCCATCATCCCTGCCCAGGTGAAGTAGCCTCCAAATCTAATGGCCCCCCAGTGCC
CACAGAGGGGGTGCCCCAGACCACAGTAGATATCCCTTCTTCCCCCCACTCAGTCCAAGA
TGTTCATGGGAGAGAAGACTTCAGGGCCTGGAAGCAGGGACTTAATTTTGAGGGGATTGC
CCGGGATCCGGGTGGATGGCACAACCACTTCAGTGACCGGATTCCGGGGGGGCCGGGGAG
CATTTCGGGCTACTGGGGCAGCTGGAGAAATTTTCGGGGAGGGGCCTGCGGAACTTCTTG
GGGAGGAACCAGATGATACCGGGTCTTAGAACCAATTGGGTGCTAGGAGGCAAAGGGGGA
CCCGAGGGCATCATAATGGCCCGTGGGAAATTGCTGCCCGGAACCCAATTAACAGGGGCC
AGGGCGCT
Restriction Sites NotI-NotI     
ACCN NM_000952
Insert Size 2000 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).
Product Components The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Reconstitution 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Reference Data
RefSeq NM_000952.3, NP_000943.1
RefSeq Size 1822 bp
RefSeq ORF 1029 bp
Locus ID 5724
Cytogenetics 1p35.3
Domains 7tm_1
Protein Families Druggable Genome, GPCR, Transmembrane
Protein Pathways Calcium signaling pathway, Neuroactive ligand-receptor interaction
Gene Summary 'This gene encodes a seven-transmembrane G-protein-coupled receptor for platelet-activating factor (PAF) that localizes to lipid rafts and/or caveolae in the cell membrane. PAF (1-0-alkyl-2-acetyl-sn-glycero-3-phosphorylcholine) is a phospholipid that plays a significant role in oncogenic transformation, tumor growth, angiogenesis, metastasis, and pro-inflammatory processes. Binding of PAF to the PAF-receptor (PAFR) stimulates numerous signal transduction pathways including phospholipase C, D, A2, mitogen-activated protein kinases (MAPKs), and the phosphatidylinositol-calcium second messenger system. Following PAFR activation, cells become rapidly desensitized and this refractory state is dependent on PAFR phosphorylation, internalization, and down-regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]'
Transcript Variant: This variant (3) lacks the 5' exon, but has an alternate 5' segment, as compared to variant 1. Variants 1-4 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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