LYVE1 anticorps

N° du produit ABIN1589924

Détail du produit anti-LYVE1 anticorps

Antigène: LYVE1 (Lymphatic Vessel Endothelial Hyaluronan Receptor 1 (LYVE1))

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp LYVE1 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (IF), Immunohistochemistry (Acetone-fixed) (IHC (af))

Fonction: Lyve-1 antibody

Specificité: Recombinant mouse soluble Lyve-1

Attributs du produit: Chromosomal location: 7, 7F2
Produced from sera of rabbits immunized with highly pure recombinant mouse soluble LYVE-1 produced in insect cells. The recombinant soluble LYVE-1 consists of amino acid 24 (Ala) to 228 (Gly) and is fused to a C-terminal His-tag (6xHis).

Purification: Protein-A purified

Immunogène: Recombinant mouse soluble Lyve-1 (ABIN1589750)

Isotype: IgG

Information d'application

Indications d'application: Western Blot: use at 2-5 μg/mL, FACS: use at 3-10 μg/mL, IF/IHC: applicable with cryo-sections.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Centrifuge vial prior to opening. Reconstitute in sterile water to a concentration of 0.1-1.0 mg/mL.

Buffer: PBS

Conseil sur la manipulation: Centrifuge vial prior to opening.

Stock: 4 °C,-20 °C

Stockage commentaire: The lyophilized antibody is stable for at least 2 years at -20°C. After sterile reconstitution the antibody is stable at 2-8°C for up to 6 months. Frozen aliquots are stable for at least 6 months when stored at -20°C. Addition of a carrier protein or 50% glycerol is recommended for frozen aliquots.

Date de péremption: 24 months

Références pour anticorps anti-LYVE1 (ABIN1589924)

Lohrberg, Wilting: "The lymphatic vascular system of the mouse head." dans: Cell and tissue research, (2016) (PubMed).

Eshita, Ji, Onishi, Kobayashi, Mizuno, Yoshida, Kubota, Onishi: "Medicinal facilities to B16F10 melanoma cells for distant metastasis control with a supramolecular complex by DEAE-dextran-MMA copolymer/paclitaxel." dans: Drug delivery and translational research, Vol. 5, Issue 1, pp. 38-50, (2015) (PubMed).

Pang, Georgoudaki, Lambut, Johansson, Tabor, Hagikura, Jin, Jansson, Alexander, Nelson, Jakobsson, Betsholtz, Sund, Karlsson, Fuxe: "TGF-?1-induced EMT promotes targeted migration of breast cancer cells through the lymphatic system by the activation of CCR7/CCL21-mediated chemotaxis." dans: Oncogene, (2015) (PubMed).

Wawrzyniak, Pich, Gross, Schütz, Fleury, Quemener, Sgandurra, Bouchaert, Moret, Mury, Rommens, Mottaz, Dombrowicz, Michalik: "Endothelial, but not smooth muscle, peroxisome proliferator-activated receptor ?/? regulates vascular permeability and anaphylaxis." dans: The Journal of allergy and clinical immunology, Vol. 135, Issue 6, pp. 1625-35.e5, (2015) (PubMed).

Grzegorek, Drozdz, Chmielewska, Gomulkiewicz, Jablonska, Piotrowska, Karczewski, Janczak, Podhorska-Okolow, Dziegiel, Szuba: "Arterial wall lymphangiogenesis is increased in the human iliac atherosclerotic arteries: involvement of CCR7 receptor." dans: Lymphatic research and biology, Vol. 12, Issue 4, pp. 222-31, (2014) (PubMed).

Quagliata, Klusmeier, Cremers, Pytowski, Harvey, Pettis, Thiele, Sleeman: "Inhibition of VEGFR-3 activation in tumor-draining lymph nodes suppresses the outgrowth of lymph node metastases in the MT-450 syngeneic rat breast cancer model." dans: Clinical & experimental metastasis, Vol. 31, Issue 3, pp. 351-65, (2014) (PubMed).

Maruyama, Maruyama, Kato, Kajiya, Moritoh, Yamamoto, Matsumoto, Sawane, Kerjaschki, Nakazawa, Kinoshita: "The effect of podoplanin inhibition on lymphangiogenesis under pathological conditions." dans: Investigative ophthalmology & visual science, Vol. 55, Issue 8, pp. 4813-22, (2014) (PubMed).

Augsten, Sjöberg, Frings, Vorrink, Frijhoff, Olsson, Borg, Östman: "Cancer-associated fibroblasts expressing CXCL14 rely upon NOS1-derived nitric oxide signaling for their tumor-supporting properties." dans: Cancer research, Vol. 74, Issue 11, pp. 2999-3010, (2014) (PubMed).

Ji, Eshita: "Rapamycin inhibition of CFA-induced lymphangiogenesis in PLN is independent of mast cells." dans: Molecular biology reports, Vol. 41, Issue 4, pp. 2217-28, (2014) (PubMed).

Padrón-Barthe, Temiño, Villa del Campo, Carramolino, Isern, Torres: "Clonal analysis identifies hemogenic endothelium as the source of the blood-endothelial common lineage in the mouse embryo." dans: Blood, Vol. 124, Issue 16, pp. 2523-32, (2014) (PubMed).

Kraima, Derks, Smit, Van Munsteren, Van der Velden, Kenter, DeRuiter: "Lymphatic drainage pathways from the cervix uteri: implications for radical hysterectomy?" dans: Gynecologic oncology, Vol. 132, Issue 1, pp. 107-13, (2014) (PubMed).

Hirosue, Vokali, Raghavan, Rincon-Restrepo, Lund, Corthésy-Henrioud, Capotosti, Halin Winter, Hugues, Swartz: "Steady-state antigen scavenging, cross-presentation, and CD8+ T cell priming: a new role for lymphatic endothelial cells." dans: Journal of immunology (Baltimore, Md. : 1950), Vol. 192, Issue 11, pp. 5002-11, (2014) (PubMed).

Berta, Hoda, Laszlo, Rozsas, Garay, Torok, Grusch, Berger, Paku, Renyi-Vamos, Masri, Tovari, Groger, Klepetko, Hegedus, Dome: "Apelin promotes lymphangiogenesis and lymph node metastasis." dans: Oncotarget, Vol. 5, Issue 12, pp. 4426-37, (2014) (PubMed).

Watari, Shibata, Kawahara, Sata, Nabeshima, Shinoda, Abe, Azuma, Murakami, Izumi, Takahashi, Kage, Kuwano, Ono: "Tumor-derived interleukin-1 promotes lymphangiogenesis and lymph node metastasis through M2-type macrophages." dans: PLoS ONE, Vol. 9, Issue 6, pp. e99568, (2014) (PubMed).

Kilarski, Muchowicz, Wachowska, M??yk-Kope?, Golab, Swartz, Nowak-Sliwinska: "Optimization and regeneration kinetics of lymphatic-specific photodynamic therapy in the mouse dermis." dans: Angiogenesis, Vol. 17, Issue 2, pp. 347-57, (2014) (PubMed).

Détails sur LYVE1

Antigène: LYVE1 (Lymphatic Vessel Endothelial Hyaluronan Receptor 1 (LYVE1))

Autre désignation: Lyve-1 (LYVE1 Produits)

Synonymes: anticorps LYVE1, anticorps XLKD1, anticorps CRSBP-1, anticorps HAR, anticorps LYVE-1, anticorps 1200012G08Rik, anticorps Crsbp-1, anticorps Lyve-1, anticorps Xlkd1, anticorps lymphatic vessel endothelial hyaluronic receptor 1a, anticorps lymphatic vessel endothelial hyaluronan receptor 1, anticorps lyve1a, anticorps LYVE1, anticorps Lyve1

Sujet: Lyve1, Xlkd1, Lyve-1, Crsbp-1, 1200012G08Rik,LYVE-1 has been identified as a major receptor for HA (extracellular matrix glycosaminoglycan hyaluronan) on the lymph vessel wall. The deduced amino acid sequence of LYVE-1 predicts a 322-residue type I integral membrane polypeptide 41 % similar to the CD44 HA receptor with a 212-residue extracellular domain containing a single Link module the prototypic HA binding domain of the Link protein superfamily. Like CD44, the LYVE-1 Molecule binds both soluble and immobilized HA. However, unlike CD44, the LYVE-1 Molecule colocalizes with HA on the luminal face of the lymph vessel wall and is completely absent from blood vessels. Hence, LYVE-1 is the first lymph-specific HA receptor to be characterized and is a uniquely powerful marker for lymph vessels themselves.

ID gène: 114332

NCBI Accession: NM_053247, NP_444477

UniProt: Q8BHC0

Pathways: Glycosaminoglycan Metabolic Process