摘要:
Certain aspects of the present invention are directed to new fully human fusion partner cell lines called human Karyochi cells, and to methods for making them. Human Karyochi cells are then fused with human antibody-secreting lymphoid cells to make fully human hybridomas called Karyochi-based hybridomas, which likewise secrete fully human monoclonal antibodies. Human Karyochi cells are made by isolating a donor nucleus that is substantially free of cytoplasm from either a first malignant B-lymphocyte cell line or a normal B-lymphocyte, and transferring the donor nucleus into the cytoplasm of a recipient cell from a second T- or B-lymphoid cell line. With time the nuclei synchronize and fuse to form the chimeric Karyochi fusion partner cell line. Nuclear transfer can be accomplished using intra-cytosolic nucleus injection or by impact-induced nucleus administration.
摘要:
Certain aspects of the present invention are directed to new fully human fusion partner cell lines called human Karyochi cells, and to methods for making them. Human Karyochi cells are then fused with human antibody-secreting lymphoid cells to make fully human hybridomas called Karyochi-based hybridomas, which likewise secrete fully human monoclonal antibodies. Human Karyochi cells are made by isolating a donor nucleus that is substantially free of cytoplasm from either a first malignant B-lymphocyte cell line or a normal B-lymphocyte, and transferring the donor nucleus into the cytoplasm of a recipient cell from a second T- or B-lymphoid cell line. With time the nuclei synchronize and fuse to form the chimeric Karyochi fusion partner cell line. Nuclear transfer can be accomplished using intra-cytosolic nucleus injection or by impact-induced nucleus administration.
摘要:
The invention is directed to a new composition for making a housing block for cryosectioning comprising agarose and optimal cutting temperature medium. The invention is further directed to new methods for making a frozen section microarray of fresh non-fixed frozen cell or tissue samples that undergo only one freeze-thaw cycle before being used in a biological assay.
摘要:
The present invention provides monoclonal antibody-producing hybridomas designated 27.F7 and 27.B1. The invention provides a method of detecting TIP-2 antigen bearing cancer cells in a sample. The invention provides a method of detecting TIP-2 antigen on the surface of cancer cells. The invention provides a method for diagnosing cancer in a subject. The invention provides a method for delivering exogenous material to TIP-2 antigen-bearing cancer cells of a human subject. The invention provides a method for treating cancer in a human subject. The invention provides isolated peptides having the amino acid sequences Lys Leu Leu Gly Gly Gln Ile Gly Leu (SEQ. ID No.) and Ser Leu Leu Gly Cys Arg His Tyr Glu Val (SEQ. ID No.). The invention provides a method for immunohistochemical screening of a tissue section for the presence of TIP-2 antigen bearing cancer cells. The invention provides a kit for detecting the presence of TIP-2 antigen-bearing cancer cells. The invention provides a method for detecting the presence of TIP-2 antigen. The invention provides a method for immunohistochemical screening of tissue sections. The invention provides a method for monitoring progression of cancer wherein the cancer cells are TIP-2 antigen-bearing cells. The invention provides a method for diagnosing cancer associated with the expression of TIP-2.
摘要翻译:本发明提供了称为27.F7和27.B1的产生单克隆抗体的杂交瘤。 本发明提供一种检测样品中携带TIP-2抗原的癌细胞的方法。 本发明提供了检测癌细胞表面的TIP-2抗原的方法。 本发明提供了一种用于诊断受试者的癌症的方法。 本发明提供了将外源性材料递送至人受试者的TIP-2抗原携带癌细胞的方法。 本发明提供了一种治疗人类受试者的癌症的方法。 本发明提供具有氨基酸序列Lys Leu Leu Gly Gly Gln Ile Gly Leu(SEQ ID NO)和Ser Leu Leu Gly Cys Arg His Tyr Glu Val的分离肽(SEQ ID NO:SEQ ID NO: 本发明提供了一种组织切片对于携带TIP-2抗原的癌细胞存在的免疫组织化学筛选方法。 本发明提供了用于检测携带TIP-2抗原的癌细胞的存在的试剂盒。 本发明提供了检测TIP-2抗原存在的方法。 本发明提供了组织切片的免疫组织化学筛选方法。 本发明提供了一种监测癌症进展的方法,其中癌细胞是携带TIP-2抗原的细胞。 本发明提供了一种诊断与TIP-2表达相关的癌症的方法。
摘要:
The present invention provides monoclonal antibody-producing hybridomas designated 27.F7 and 27.B1. The invention provides a method of detecting TIP-2 antigen bearing cancer cells in a sample. The invention provides a method of detecting TIP-2 antigen on the surface of cancer cells. The invention provides a method for diagnosing cancer in a subject. The invention provides a method for delivering exogenous material to TIP-2 antigen-bearing cancer cells of a human subject. The invention provides a method for treating cancer in a human subject. The invention provides isolated peptides having the amino acid sequences Lys Leu Leu Gly Gly Gln Ile Gly Leu (SEQ. ID No.) and Ser Leu Leu Gly Cys Arg His Tyr Glu Val (SEQ. ID No.). The invention provides a method for immunohistochemical screening of a tissue section for the presence of TIP-2 antigen bearing cancer cells. The invention provides a kit for detecting the presence of TIP-2 antigen-bearing cancer cells. The invention provides a method for detecting the presence of TIP-2 antigen. The invention provides a method for immunohistochemical screening of tissue sections. The invention provides a method for monitoring progression of cancer wherein the cancer cells are TIP-2 antigen-bearing cells. The invention provides a method for diagnosing cancer associated with the expression of TIP-2.
摘要翻译:本发明提供了称为27.F7和27.B1的产生单克隆抗体的杂交瘤。 本发明提供一种检测样品中携带TIP-2抗原的癌细胞的方法。 本发明提供了检测癌细胞表面的TIP-2抗原的方法。 本发明提供了一种用于诊断受试者的癌症的方法。 本发明提供了将外源性材料递送至人受试者的TIP-2抗原携带癌细胞的方法。 本发明提供了一种治疗人类受试者的癌症的方法。 本发明提供具有氨基酸序列Lys Leu Leu Gly Gly Gln Ile Gly Leu(SEQ ID NO)和Ser Leu Leu Gly Cys Arg His Tyr Glu Val的分离肽(SEQ ID NO:SEQ ID NO: 本发明提供了一种组织切片对于携带TIP-2抗原的癌细胞存在的免疫组织化学筛选方法。 本发明提供了用于检测携带TIP-2抗原的癌细胞的存在的试剂盒。 本发明提供了检测TIP-2抗原存在的方法。 本发明提供了组织切片的免疫组织化学筛选方法。 本发明提供了一种监测癌症进展的方法,其中癌细胞是携带TIP-2抗原的细胞。 本发明提供了一种诊断与TIP-2表达相关的癌症的方法。
摘要:
This invention provides monoclonal antibody-producing hybridomas designated 27.F7 and 27.B1. The invention also provides methods for detecting TIP-2 antigen-bearing cancer cells in a sample, detecting the presence of TIP-2 antigen, optionally on the surface of cancer cells, immunohistochemical screening of a tissue section for the presence of TIP-2 antigen bearing cancer cells, diagnosing cancer in a subject, monitoring progression of cancer wherein the cancer cells are TIP-2 antigen-bearing cells, delivering exogenous material to TIP-2 antigen-bearing cancer cells of a human subject, and treating cancer in a human subject. This invention further provides a kit for detecting the presence of TIP-2 antigen-bearing cancer cells. This invention also provides isolated peptides having the amino acid sequences Lys Leu Leu Gly Gly Gln Ile Gly Leu (SEQ ID No:3) and Ser Leu Leu Gly Cys Arg His Tyr Glu Val (SEQ ID NO:4).
摘要翻译:本发明提供了称为27.F7和27.B1的产生单克隆抗体的杂交瘤。 本发明还提供了用于检测样品中TIP-2抗原的癌细胞的方法,任选地在癌细胞表面检测TIP-2抗原的存在,组织切片的TIP-2抗原的存在的免疫组织化学筛选 诊断受试者中的癌症,监测癌症的进展,其中癌细胞是TIP-2抗原携带细胞,将外源性物质递送到人受试者的TIP-2抗原携带癌细胞,以及治疗人类的癌症 学科。 本发明还提供了用于检测携带TIP-2抗原的癌细胞的存在的试剂盒。 本发明还提供了具有氨基酸序列Lys Leu Leu Gly Gly Gln Ile Gly Leu(SEQ ID No.3)和Ser Leu Leu Gly Cys Arg His Tyr Glu Val(SEQ ID NO:4)的分离肽。
摘要:
The present invention provides a trioma cell which does not produce any antibody obtained by fusing a hetermomyeloma cell which does not produce any antibody with a human lymphoid cell, wherein the heteromyeloma cell is designated B6B11. The invention also provides a tetroma cell capable of producing a monoclonal antibody having specific binding affinity for an antigen obtained by fusing a trioma cell which does not produce any antibody with a human lymphoid cell capable of producing antibody having specific binding affinity for the antigen. The invention also provides methods for generating trioma cells and tetroma cells, and the cells generated by the methods.
摘要:
Techniques for applying torque to microscopic paramagnetic structures in a body includes exposing a body simultaneously to a first magnetic field oscillating at a first frequency in a first direction and a different second magnetic field oscillating at a second frequency in a second direction. The body includes a plurality of microscopic paramagnetic structures for which magnetic susceptibility to the first magnetic field is different from magnetic susceptibility to the second magnetic field. Such techniques are effective for ameliorating a symptom of a disease in an animal in which disease agents or diseased cells selectively include microscopic paramagnetic structures, including malaria.
摘要:
The present invention provides a heteromyeloma cell other than B6B11, capable of producing a trioma cell when fused with a human lymphoid cell, wherein the trioma cell is capable of producing a tetroma cell capable of producing a monoclonal antibody having specific binding affinity for an antigen, when fused with a second human lymphoid cell, the second human lymphoid cell being capable of producing antibody having specific binding affinity for the antigen. The invention provides a trioma cell fusion partner which does not produce any antibody obtained by fusing a hetermomyeloma cell which does not produce any antibody with a human lymphoid cell. The invention provides a tetroma cell capable of producing a monoclonal antibody having specific binding affinity for an antigen obtained by fusing a trioma cell which does not produce any antibody with a human lymphoid cell capable of producing antibody having specific binding affinity for the antigen. The invention provides a method of producing a monoclonal antibody specific for an antigen associated with a condition. The invention provides a method of identifying an antigen associated with a condition using the trioma fusion partner. The invention provides a method of diagnosing a condition using the trioma fusion partner. The invention provides a method for preventing a condition. Compositions and therapeutic compositions are also provided, using monoclonal antibodies produced using the trioma fusion partner.
摘要:
This invention provides: a heteromyeloma, other than B6B11, capable of producing a trioma when fused with a human lymphoid cell, wherein the trioma is capable of producing a monoclonal antibody-secreting tetroma when fused with a second, antibody-secreting human lymphoid cell; a trioma fusion partner which does not produce antibody, obtained by fusing a heteromyeloma which does not produce antibody with a human lymphoid cell; a monoclonal antibody-secreting tetroma, obtained by fusing a trioma which does not produce antibody with an antibody-secreting human lymphoid cell; a method of producing a monoclonal antibody that specifically recognizes an antigen associated with a condition; a method of identifying an antigen associated with a condition using the trioma fusion partner; a method of diagnosing a condition using the trioma fusion partner; a method for preventing a condition; and compositions and therapeutic compositions comprising monoclonal antibodies produced using the trioma fusion partner.