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LYVE1 抗体

This 兔 多克隆 antibody specifically detects LYVE1 in WB, FACS, IF 和 IHC (af). It exhibits reactivity toward 小鼠. It has been mentioned in 15+ publications
产品编号 ABIN1589924
发货至: 中国
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for LYVE1 抗体 (ABIN1589924)

抗原

See all LYVE1 抗体
LYVE1 (Lymphatic Vessel Endothelial Hyaluronan Receptor 1 (LYVE1))

适用

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小鼠

宿主

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克隆类型

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多克隆

标记

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This LYVE1 antibody is un-conjugated

应用范围

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

    Lyve-1 antibody

    特异性

    Recombinant mouse soluble Lyve-1

    产品特性

    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).

    纯化方法

    Protein-A purified

    免疫原

    Recombinant mouse soluble Lyve-1 (ABIN1589750)

    亚型

    IgG
  • 应用备注

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

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

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

    缓冲液

    PBS

    注意事项

    Centrifuge vial prior to opening.

    储存条件

    4 °C,-20 °C

    储存方法

    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.

    有效期

    24 months
  • Lohrberg, Wilting: "The lymphatic vascular system of the mouse head." in: 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." in: 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." in: 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." in: 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." in: 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." in: 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." in: 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." in: 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." in: 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." in: 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?" in: 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." in: 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." in: 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." in: 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." in: Angiogenesis, Vol. 17, Issue 2, pp. 347-57, (2014) (PubMed).

  • 抗原

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

    别名

    Lyve-1

    背景

    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.

    基因ID

    114332

    NCBI登录号

    NM_053247, NP_444477

    UniProt

    Q8BHC0

    途径

    Glycosaminoglycan Metabolic Process
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