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Merck
CN

L2139

Lipoprotein, low density from human plasma

buffered aqueous solution, from human plasma

Synonym(s):

β-Lipoprotein, LDL, Low density lipoprotein

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About This Item

CAS Number:
UNSPSC Code:
12352200
EC Number:
294-482-1
MDL number:
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biological source

human plasma

sterility

0.22 μm filtered

form

buffered aqueous solution

shipped in

wet ice

storage temp.

2-8°C

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General description

Low density lipoproteins are smaller than VLDL and IDL (26 nm) (MW approximately 3.5 million) and more dense (~1.04). The protein component of LDL is apolipoprotein B100. LDL contains 20-22% protein, 10-15% triglycerides, 20-28% phospholipids, 37-48% cholesteryl esters and 8-10% cholesterol.

Biochem/physiol Actions

LDL and HDL transport both dietary and endogenous cholesterol in the plasma. LDL is the main transporter of cholesterol and cholesteryl esters and makes up more than half of the total lipoprotein in plasma. LDL is absorbed by the liver and other tissues via receptor mediated endocytosis. The cytoplasmic domain of the LDL receptor facilitates the formation of coated pits; receptor-rich regions of the membrane. The ligand binding domain of the receptor recognizes apo-B100 on LDL, resulting in the formation of a clathrin-coated vesicle. ATP-dependent proton pumps lower the pH inside the vesicle resulting dissociation of LDL from its receptor. After loss of the clathrin coat the vesicles fuse with lysozomes, resulting in peptide and cholesteryl ester enzymatic hydrolysis. The LDL receptor can be recycled to the cell membrane. Insulin, tri-iodothyronine and dexamethasome have shown to be involved with the regulation of LDL receptor mediated uptake.

Packaging

Package size based on protein content

Physical form

Solution in 0.15 M NaCl with 0.01% EDTA, pH 7.4

Disclaimer

Freezing may cause denaturation.

Regulatory Information

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Alina A Constantinescu et al.
Arteriosclerosis, thrombosis, and vascular biology, 23(9), 1541-1547 (2003-07-12)
A thick endothelial glycocalyx provides the endothelial surface with a nonadherent shield. Oxidized LDL (Ox-LDL) degrades the endothelial glycocalyx. We hypothesized that glycocalyx degradation stimulates leukocyte-endothelial cell adhesion, whereas intravascular supplementation with sulfated polysaccharides reconstitutes the endothelial glycocalyx and attenuates
G Krystal et al.
The Journal of experimental medicine, 180(3), 851-860 (1994-09-01)
Normal human bone marrow cells, highly enriched for burst-forming units-erythroid (BFU-E), were cultured in serum-free medium, in the presence and absence of various factors, to investigate the mechanisms involved in regulating erythroid differentiation. In cultures containing interleukin 3 (IL-3), Steel
H Vink et al.
Circulation, 101(13), 1500-1502 (2000-04-04)
Flowing erythrocytes and platelets are separated from the luminal endothelial cell (EC) surface by a 0.5-microm-wide space named the endothelial surface layer. We hypothesized that the disruption of the endothelial surface layer by oxidized low-density lipoproteins (Ox-LDL) contributes to atherogenic
Douglas C Dooley et al.
Methods in molecular biology (Clifton, N.J.), 263, 201-218 (2004-02-21)
Methods are described for the characterization of CD34 antigen modulation and its relationship to cell proliferation in early human hematopoietic cells. Toward that end, quiescent primitive CD34+ and CD34NEG cells are purified from mobilized peripheral blood (MoPB). Unlike CD34NEG cells
Murat O Arcasoy et al.
British journal of haematology, 130(1), 121-129 (2005-06-29)
The regeneration of circulating red blood cells in response to anaemia associated with blood loss or haemolysis involves an increased rate of erythropoiesis and expansion of proerythroblasts, the bone marrow precursor cells that terminally differentiate into mature erythrocytes. This study

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