LDL Receptor (LDLR) (NM_000527) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC200006L1V

  • LentiORF®

Lenti ORF particles, LDLR (Myc-DDK tagged) - Human low density lipoprotein receptor (LDLR), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 8,930.00


货期*
详询

规格
    • 200 ul

Cited in 1 publication.

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Specifications

Product Data
Product Name LDL Receptor (LDLR) (NM_000527) Human Tagged ORF Clone Lentiviral Particle
Synonyms FH; FHC; FHCL1; LDLCQ2
Vector pLenti-C-Myc-DDK
ACCN NM_000527
ORF Size 2580 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC200006).
OTI Disclaimer 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
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Reference Data
RefSeq NM_000527.2, NP_000518.1
RefSeq Size 5175 bp
RefSeq ORF 2583 bp
Locus ID 3949
Domains ldl_recept_b, EGF_CA, ldl_recept_a, EGF, EGF
Protein Families Druggable Genome, ES Cell Differentiation/IPS, Transmembrane
Protein Pathways Endocytosis
MW 95.38 kDa
Gene Summary The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. Low density lipoprotein (LDL) is normally bound at the cell membrane and taken into the cell ending up in lysosomes where the protein is degraded and the cholesterol is made available for repression of microsomal enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase, the rate-limiting step in cholesterol synthesis. At the same time, a reciprocal stimulation of cholesterol ester synthesis takes place. Mutations in this gene cause the autosomal dominant disorder, familial hypercholesterolemia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010]
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Citations (1)

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