Merck Millipore代理MABS26 Anti-LDLR Antibody, clone C7;store at +2℃ to +8℃

2025-06-28

货号:MABS26

品牌:Merck Millipore

规格:100Ug

目录价:¥4438.00

市场价格:¥3772.30

会员价格:¥3550.40

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-LDLR Antibody, clone C7 | MABS26 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Specificity: This antibody recognizes LDLR. View All» Molecular Weight: 160 kDa Observed The translation of LDLR mRNA yields a 120 kDa protein that is post-translationally modified in the Golgi apparatus into the mature, 160 kDa LDLR. (Tolleshaug, H., et al. (1982). Cell 30:715–724.) View All» Immunogen: Partially purified bovine adrenal LDL receptor View All» Clone: C7 View All» Isotype: IgG2bκ View All» Background Information: Low-Density Lipoprotein (LDL) Receptor is a mosaic protein 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). Mutations in LDLR are associated with familial hypercholesterolemia which is characterized by high levels of LDL in the blood. View All» Species Reactivity:

  • Human

  • Bovine

    View All» Species Reactivity Note: Demonstrated to react with human. Predicted to react with bovine based on 100% sequence homology. View All» Control: ARPE-19 cell lysate View All» Quality Assurance: Evaluated by Western Blot in ARPE-19 cell lysate.Western Blot Analysis: 1 µg/mL of this antibody detected LDLR on 10 µg of ARPE-19 cell lysate. View All» Purification Method: Protein G purfied View All» Presentation: Purified mouse monoclonal IgG2bκ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide. View All» Storage Conditions: Stable for 1 year at 2-8°C from date of receipt. View All» UniProt Number: P01131 View All» Entrez Gene Number: NP_001160002 View All» Gene Symbol:
    • LDLR

    • LDLCQ2

    • FH

    • FHC

      View All» Alternate Names:
      • low density lipoprotein receptor

      • LDL receptor

        View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» Key Applications: Western Blotting View All» Entrez 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. [provided by RefSeq]. View All» UniProt Summary: FUNCTION: SwissProt: P01130 # Binds LDL, the major cholesterol-carrying lipoprotein of plasma, and transports it into cells by endocytosis. In order to be internalized, the receptor-ligand complexes must first cluster into clathrin-coated pits. In case of HIV-1 infection, functions as a receptor for extracellular Tat in neurons, mediating its internalization in uninfected cells.SIZE: 860 amino acids; 95376 Da SUBUNIT: Interacts with LDLRAP1. Interacts with SNX17. Interacts with HCV E1/E2 heterodimer. Interacts with HIV-1 Tat.SUBCELLULAR LOCATION: Membrane; Single-pass type I membrane protein.PTM: N- and O-glycosylated.DISEASE: SwissProt: P01130 # Defects in LDLR are the cause of familial hypercholesterolemia (FH) [MIM:143890]; a common autosomal semi- dominant disease that affects about 1 in 500 individuals. The receptor defect impairs the catabolism of LDL, and the resultant elevation in plasma LDL-cholesterol promotes deposition of cholesterol in the skin (xanthelasma), tendons (xanthomas), and coronary arteries (atherosclerosis).SIMILARITY: SwissProt: P01130 ## Belongs to the LDLR family. & Contains 3 EGF-like domains. & Contains 7 LDL-receptor class A domains. & Contains 6 LDL-receptor class B repeats. View All» Product Name: Anti-LDLR, clone C7 View All» Concentration: 1.0 mg/mL View All» Antibody Type: Monoclonal Antibody View All» Qty/Pk: 100 μg View All» Format: Purified View All» Host: Mouse View All»

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