PLTP (NM_006227) Human Untagged Clone

CAT#: SC116234

PLTP (untagged)-Human phospholipid transfer protein (PLTP), transcript variant 1


  "NM_006227" in other vectors (7)

Reconstitution Protocol

USD 457.00

In Stock*

Size
    • 10 ug

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Frequently bought together (3)
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Other products for "PLTP"

Specifications

Product Data
Type Human Untagged Clone
Tag Tag Free
Symbol PLTP
Synonyms BPIFE; HDLCQ9
Vector pCMV6-XL5
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
>OriGene ORF within SC116234 sequence for NM_006227 edited (data generated by NextGen Sequencing)
ATGGCCCTCTTCGGGGCCCTCTTCCTAGCGCTGCTGGCAGGCGCACATGCAGAGTTCCCA
GGCTGCAAGATCCGCGTCACCTCCAAGGCGCTGGAGCTGGTGAAGCAGGAGGGGCTGCGC
TTTCTGGAGCAAGAGCTGGAGACTATCACCATTCCGGACCTGCGGGGCAAAGAAGGCCAC
TTCTACTACAACATCTCTGAGGTGAAGGTCACAGAGCTGCAACTGACATCTTCCGAGCTC
GATTTCCAGCCACAGCAGGAGCTGATGCTTCAAATCACCAATGCCTCCTTGGGGCTGCGC
TTCCGGAGACAGCTGCTCTACTGGTTCTTCTATGATGGGGGCTACATCAACGCCTCAGCT
GAGGGTGTGTCCATCCGCACTGGTCTGGAGCTCTCCCGGGATCCCGCTGGACGGATGAAA
GTGTCCAATGTCTCCTGCCAGGCCTCTGTCTCCAGAATGCACGCGGCCTTCGGGGGAACC
TTCAAGAAGGTGTATGATTTTCTCTCCACGTTCATCACCTCAGGGATGCGCTTCCTCCTC
AACCAGCAGATCTGCCCTGTCCTCTACCACGCAGGGACGGTCCTGCTCAACTCCCTCCTG
GACACCGTGCCTGTGCGCAGTTCTGTGGACGAGCTTGTTGGCATTGACTATTCCCTCATG
AAGGATCCTGTGGCTTCCACCAGCAACCTGGACATGGACTTCCGGGGGGCCTTCTTCCCC
CTGACTGAGAGGAACTGGAGCCTCCCCAACCGGGCAGTGGAGCCCCAGCTGCAGGAGGAA
GAGCGGATGGTGTATGTGGCCTTCTCTGAGTTCTTCTTCGACTCTGCCATGGAGAGCTAC
TTCCGGGCGGGGGCCCTGCAGCTGTTGCTGGTGGGGGACAAGGTGCCCCACGACCTGGAC
ATGCTGCTGAGGGCCACCTACTTTGGGAGCATTGTCCTGCTGAGCCCAGCAGTGATTGAC
TCCCCATTGAAGCTGGAGCTGCGGGTCCTGGCCCCACCGCGCTGCACCATCAAGCCCTCT
GGCACCACCATCTCTGTCACTGCTAGCGTCACCATTGCCCTGGTCCCACCAGACCAGCCT
GAGGTCCAGCTGTCCAGCATGACTATGGACGCCCGTCTCAGCGCCAAGATGGCTCTCCGG
GGGAAGGCCCTGCGCACGCAGCTGGACCTGCGCAGGTTCCGAATCTATTCCAACCATTCT
GCACTGGAGTCGCTGGCTCTGATCCCATTACAGGCCCCTCTGAAGACCATGCTGCAGATT
GGGGTGATGCCCATGCTCAATGAGCGGACCTGGCGTGGGGTGCAGATCCCACTACCTGAG
GGCATCAACTTTGTGCATGAGGTGGTGACGAACCATGCGGGATTCCTCACCATCGGGGCT
GATCTCCACTTTGCCAAAGGGCTGCGAGAGGTGATTGAGAAGAACCGGCCTGCTGATGTC
AGGGCGTCCACTGCCCCCACACCGTCCACAGCAGCTGTCTGA

Clone variation with respect to NM_006227.3
>OriGene 5' read for NM_006227 unedited
TCAGAATTTTGTAATACGACTTCACTATAGGGCGGCCGCGAATCGGCACGAGGGAGCTGC
CCGCCATCCCACGTGACCGCGCCGCCCCCCAGCTCCACCGCTGAGCCCGCTCGCCATGGC
CCTCTTCGGGGCCCTCTTCCTAGCGCTGCTGGCAGGCGCACATGCAGAGTTCCCAGGCTG
CAAGATCCGCGTCACCTCCAAGGCGCTGGAGCTGGTGAAGCAGGAGGGGCTGCGCTTTCT
GGAGCAAGAGCTGGAGACTATCACCATTCCGGACCTGCGGGGCAAAGAAGGCCACTTCTA
CTACAACATCTCTGAGGTGAAGGTCACAGAGCTGCAACTGACATCTTCCGAGCTCGATTT
CCAGCCACAGCAGGAGCTGATGCTTCAAATCACCAATGCCTCCTTGGGGCTGCGCTTCCG
GAGACAGCTGCTCTACTGGTTCTTCTATGATGGGGGCTACATCAACGCCTCAGCTGAGGG
TGTGTCCATCCGCACTGGTCTGGAGCTCTCCCGGGATCCCGCTGGACGGATGAAAGTGTC
CAATGTCTCCTGCCAGGCCTCTGTCTCCAGAATGCACGCGGCCTTCGGGGGAACCTTCAA
GAAGGTGTATGATTTTCTCTCCACGTTCATCACCTCAGGGATGCGCTTCCTCCTCAACCA
GCAGATCTGCCCTGTCCTCTACCACGCAGGNACGGTCCTGCTCAACTCCCTCCTGGACAC
CGTGCCTGTGCGCAGTTCTGTGGACGAGCTTGTTGGCATTGACTATTCCCTCATGAAGGA
TCCTGTGGGCTCCACCAGNCACCTGGACATGGACTTCCGGNGGGCCCTCTTTCCCCTGAC
TGANAGGAACTGGAGCCTNCCCACCGGGCAGTGGAGCCCCACTGCNAGAGAANAACGNAT
GGTGTATGTGGCCTTCTCTGAGTCTTCTCGATCTGCCT
>OriGene 3' read for NM_006227 unedited
CGCAATCTAGAGTCGAGTTTTTTTTTTTTTTTTTTGGTGGTGGACGGACTGTAATTGATA
GATTGATTATGGAATTAAATTGGGTACAGCTTCAAATCCCGTCTTCTCTGTGGCACTGGG
GGTTAGAGGGGGCACTACAGGCTATGAATGTGGGAAAAGAGGGGCTGAGAGGGGTTGGGG
TCCTGAATGACAGCTGCCAGCTTGGGGATTGAGGGCTCAAACAGCTGCTGTGGACGGTGT
GGGGGCAGTGGACGCCCTGACATCAGCAGGCCGGTTCTTCTCAATCACCTCTCGCAGCCC
TTTGGCAAAGTGGAGATCAGCCCCGATGGTGAGGAATCCCGCATGGTTCGTCACCACCTC
ATGCACAAAGTTGATGCCCTCAGGTAGTGGGATCTGCACCCCACGCCAGGTCCGCTCATT
GAGCATGGGCATCACCCCAATCTGCAGCATGGTCTTCAGAGGGGCCTGTAATGGGATCAG
AGCCAGCGACTCCAGTGCAGAATGGTTGGAATAGATTCGGAACCTGCGCAGGTCCAGCTG
CGTGCGCAGGGCCTTCCCCCGAGAGCCATCTTGGCGCTGAGACGGGCGTCCATAGTCATG
CTGGACAGCTGGACCTCANGCTGGTCTGGTGGGACCAGNNGCATGGTGACGCTAGCAGTG
ACAGAGATGGTGGTGCCANAGGGCTTGATGGTGCANCGCGGTGGGGCCAGAACCCGCAGC
TNCAGCTTCAATGGGGAGTCAATCACTGCTGGGCTCAGCAGGACAATGCTNCCAAAAGTA
GTGGCCCTCAACCACATGTCCAGNTCGTGGGGCACCTTGTCCCCCACCAGCACAGCTGCA
GGGCCCCCGCCCGGAGTAGCTCTCCATGCAAGTCGAGAAGACTCANAGAGGCCCATACCC
ATCGTCTTNCTCTGCANTGGGCTCCATGCCCGNTGGGAAGCTCCATTCTTTAGCANGGGA
AAAGCCCCCGGAGTCATTCAGTTCTGTGGAGCCAGATCTCTTAGA
Restriction Sites ECoRI-NOT     
ACCN NM_006227
Insert Size 2060 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 ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
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_006227.2, NP_006218.1
RefSeq Size 1745 bp
RefSeq ORF 1482 bp
Locus ID 5360
UniProt ID P55058
Cytogenetics 20q13.12
Domains BPI1
Protein Families Druggable Genome, Secreted Protein
Protein Pathways PPAR signaling pathway
Gene Summary The protein encoded by this gene is one of at least two lipid transfer proteins found in human plasma. The encoded protein transfers phospholipids from triglyceride-rich lipoproteins to high density lipoprotein (HDL). In addition to regulating the size of HDL particles, this protein may be involved in cholesterol metabolism. At least two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Transcript Variant: This variant (1) encodes the predominant isoform (a). 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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