Recombinant Cynomolgus LDLR protein, His-tagged
Cat.No. : | LDLR-366C |
Product Overview : | Recombinant Cynomolgus LDLR protein (Ala22-Gly788), fused to His tag at C-terminus, was expressed in human 293 cells (HEK293). |
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Description : | Low-Density Lipoprotein (LDL) Receptor is also known as LDLR, FH, FHC, LDLCQ2, and is a mosaic protein of ~840 amino acids (after removal of signal peptide) that mediates the endocytosis of cholesterol-rich LDL. It is a cell-surface receptor that recognizes the apoprotein B100 which is embedded in the phospholipid outer layer of LDL particles. The receptor also recognizes the apoE protein found in chylomicron remnants and VLDL remnants (IDL). It belongs to the Low density lipoprotein receptor gene family. LDL receptor complexes are present in clathrin-coated pits (or buds) on the cell surface, which when bound to LDL-cholesterol via adaptin, are pinched off to form clathrin-coated vesicles inside the cell. This allows LDL-cholesterol to be bound and internalized in a process known as endocytosis and prevents the LDL just diffusing around the membrane surface. This occurs in all nucleated cells (not erythrocytes), but mainly in the liver which removes ~70% of LDL from the circulation. Synthesis of receptors in the cell is regulated by the level of free intracellular cholesterol; if it is in excess for the needs of the cell then the transcription of the receptor gene will be inhibited. LDL receptors are translated by ribosomes on the endoplasmic reticulum and are modified by the Golgi apparatus before travelling in vesicles to the cell surface. LDL is directly involved in the development of atherosclerosis, due to accumulation of LDL-cholesterol in the blood. Atherosclerosis is the process responsible for the majority of cardiovascular diseases. |
Source : | HEK293 |
Species : | Cynomolgus |
Tag : | His |
Form : | Lyophilized from 0.22 um filtered solution in PBS, pH7.4, 10% trehalose. |
Molecular Mass : | The protein has a calculated MW of 86.8 kDa. The protein migrates as 135-155 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation. |
Protein length : | 767 |
Endotoxin : | Less than 1.0 EU per ug by the LAL method. |
Purity : | >95% as determined by SDS-PAGE. |
Storage : | For long term storage, the product should be stored at lyophilized state at -20 centigrade or lower. Please avoid repeated freeze-thaw cycles. This product is stable after storage at: -20 centigrade to -70 centigrade for 12 months in lyophilized state; -70 centigrade for 3 months under sterile conditions after reconstitution. |
Reconstitution : | It is recommended that sterile water be added to the vial to prepare a stock solution of 0.2 ug/ul. Centrifuge the vial at 4℃ before opening to recover the entire contents. |
Gene Name : | LDLR |
Official Symbol : | LDLR |
Synonyms : | FH; FHC; LDLCQ2 |
Gene ID : | 102127361 |
mRNA Refseq : | XM_005587996.2 |
Protein Refseq : | XP_005588053.1 |
UniProt ID : | A0A2K5VYW3 |
Products Types
◆ Recombinant Protein | ||
LDLR-2947C | Recombinant Cynomolgus LDLR protein, His-tagged | +Inquiry |
LDLR-798H | Recombinant Human LDLR protein(Met1-Arg788), His-tagged | +Inquiry |
LDLR-267H | Recombinant Human LDLR protein, His-Avi-tagged, Biotinylated | +Inquiry |
Ldlr-3283M | Recombinant Mouse Ldlr protein(Met1-Arg790), His-tagged | +Inquiry |
LDLR-347H | Recombinant Human LDLR Protein, His-tagged | +Inquiry |
◆ Native Protein | ||
LDLR-85H | Native Human Lipoprotein | +Inquiry |
◆ Lysates | ||
LDLR-2762MCL | Recombinant Mouse LDLR cell lysate | +Inquiry |
LDLR-2780HCL | Recombinant Human LDLR cell lysate | +Inquiry |
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Not For Human Consumption!
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Customer Reviews (3)
Write a reviewThe LDLR protein stands out for its exceptional quality, making it an excellent choice to meet my experimental requirements.
Its purity and consistency guarantee reliable and reproducible results, ensuring the reliability of my research outcomes.
the LDLR protein offers superior quality and reliability, making it a perfect fit for my experimental needs.
Q&As (5)
Ask a questionYes, conditions where increasing the expression or function of LDLR could potentially aid in reducing circulating LDL cholesterol and minimizing cardiovascular risk.
Yes, research is continually conducted to better understand LDLR-related conditions and to develop more effective treatments, including gene-editing technologies and novel therapies.
Dysfunction in LDLR can lead to high levels of LDL cholesterol in the blood, contributing to conditions like familial hypercholesterolemia and an increased risk of heart disease.
A dysfunctional LDLR can lead to an accumulation of LDL cholesterol in the arteries, promoting atherosclerosis, the hardening and narrowing of arteries.
Treatments involve lifestyle changes, cholesterol-lowering medications, and in some cases, gene therapies or specialized medications targeting the LDL receptor.
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