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Hermes-3细胞

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产品名称: Hermes-3细胞
产品型号: Hermes-3
产品展商: HZbscience
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简单介绍

Hermes-3细胞应如何避免细胞污染,细胞污染的种类可分成**、酵母菌、霉菌、病毒和霉浆菌。主要的污染原因为无菌操作技术不当、操作室环境不佳、污染之血清和污染之细胞等。严格之无菌操作技术、清洁的环境、与品质良好之细胞来源和培养基配制是减低污染之*好方法。Hermes-3细胞何时须更换培养基?视细胞生长密度而定,或遵照细胞株基本数据上之更换时间,按时更换培养基即可。


Hermes-3细胞  的详细介绍

Hermes-3细胞

细胞形态: **样

**类型: IgG2a

运输方式: 冻存运输

数量: 大量

ATCC Number: HB-9480™

生长状态: 悬浮生长

是否是肿瘤细胞: 0

物种来源: 小鼠

Designations: Hermes-3

Hermes-3细胞Depositors: Stanford University Board of Trustees

Isotype: IgG2a

Biosafety Level: 1

Shipped: frozen

Medium & Serum: See Propagation

Growth Properties: suspension

Organism: Mus musculus (B cell); Mus musculus (myeloma) deposited as mouse (B cell); mouse (myeloma)

Morphology: lymphoblast


Source: Cell Type: hybridoma: B lymphocyte;

Cellular Products: immunoglobulin; monoclonal antibody; against human Peyer's patch endothelial cells (CD44)

Permits/Forms: Hermes-3细胞In addition to the MTA mentioned above, other ATCC and/or regulatory permits may be required for the transfer of this ATCC material. Anyone purchasing ATCC material is ultimately responsible for obtaining the permits. Please click here for information regarding the specific requirements for shipment to your location.

Applications: The antibody specifically inhibits lymphocyte adhesion to human mucosal high endothelial venules (HEV).

It binds to an extracellular site on CD44, proximal to the hyaluronate binding site and distal to the sites of variant exon splicing.

Comments: Animals were immunized with.

Spleen cells were fused with myeloma cells.

The antibody specifically inhibits lymphocyte adhesion to human mucosal high endothelial venules (HEV).

It binds to an extracellular site on CD44, proximal to the hyaluronate binding site and distal to the sites of variant exon splicing.

It does not inhibit lymphocyte binding to hyaluronate.

Propagation: ATCC complete growth medium: HB101 medium, 100% - OR - RPMI 1640 medium, 90%; fetal bovine serum, 10%

Subculturing: Hermes-3细胞Medium Renewal: Every 2 to 3 days

Cultures can be maintained by addition or replacement of fresh medium. Start cultures at 2 X 10 exp5 cells/ml and maintain between 1 X 10 exp5 and 1 X 10 exp6 cells/ml.

References: 22068: Butcher EC. Method to control leukocyte extravasation. US Patent 5,403,919 dated Apr 4 1995

22799: Jalkanen S, et al. Lymphocyte recognition of high endothelium: antibodies to distinct epitopes of an 85-95-kD glycoprotein antigen differentially inhibit lymphocyte binding to lymph node, mucosal, or synovial endothelial cells. J. Cell Biol. 105: 983-990, 1987. PubMed: 2442176

22800: Picker LJ, et al. Monoclonal antibodies to human lymphocyte homing receptors define a novel class of adhesion molecules on diverse cell types. J. Cell Biol. 109: 927-937, 1989. PubMed: 2474557

23155: Vogel H, et al. H-CAM expression in the human nervous system: evidence for a role in diverse glial interactions. J. Neurocytol. 21: 363-373, 1992. PubMed: 1607880

23176: Jalkanen ST, et al. A lymphoid cell surface glycoprotein involved in endothelial cell recognition and lymphocyte homing in man. Eur. J. Immunol. 16: 1195-1202, 1986. PubMed: 2429846

23387: Butcher EC. Hermes-3细胞Specificity of leukocyte-endothelial interactions and diapedesis: physiologic and therapeutic implications of an active decision process. Res. Immunol. 144: 695-698, 1993. PubMed: 8159870

23473: Picker LJ, et al. Monoclonal antibodies against the CD44 [In(Lu)-related p80], and Pgp-1 antigens in man recognize the Hermes class of lymphocyte homing receptors. J. Immunol. 142: 2046-2051, 1989. PubMed: 2646376

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