摘要:
The invention is directed to a method for enriching target cells from a sample of cells characterized by: a) contacting the sample with a cell aggregation agent and first magnetic particles having an iron content of 0.1 pg to 5000 pg, coupled to a first antigen recognizing moiety; and second magnetic particles having an iron content of 0.05 fg to 100 fg and coupled to a second antigen recognizing moiety to obtain mixture a) b) applying a first magnetic field gradient to the mixture a) thereby removing the cells bound to the first antigen recognizing moiety coupled to the first magnetic particles, to obtain a mixture b) and obtaining an agglomerate comprising the cells of mixture a) bound to the cell aggregation agent c) applying a second magnetic field gradient to the mixture b) thereby immobilizing the cells bound to the second antigen recognizing moiety coupled to the second magnetic particles d) recovering the immobilized cells from the second magnetic field gradient as target cells.
摘要:
The present invention provides a humanized antibody or fragment thereof specific for the antigen CD45R0, wherein said antibody or fragment thereof comprises a humanized heavy chain variable domain comprising a CDR1 region of SEQ ID NO:1, a CDR2 region of SEQ ID NO:2, and a CDR3 region of SEQ ID NO:3, and a humanized light chain variable domain comprising a CDR1 region of SEQ ID NO:4, a CDR2 region of SEQ ID NO:5, and a CDR3 region of SEQ ID NO:6. It is also provided the use of the present antibody or fragment thereof for enrichment or depletion of CD45R0-expressing cells from a sample comprising CD45R0-expressing cells.
摘要翻译:本发明提供对抗原CD45R0特异性的人源化抗体或其片段,其中所述抗体或其片段包含人源化重链可变结构域,其包含SEQ ID NO:1的CDR1区,SEQ ID NO:2的CDR2区, 和SEQ ID NO:3的CDR3区,以及包含SEQ ID NO:4的CDR1区,SEQ ID NO:5的CDR2区和SEQ ID NO:6的CDR3区的人源化轻链可变结构域。 还提供了本抗体或其片段用于从包含CD45R0表达细胞的样品中富集或消耗表达CD45R0的细胞的用途。
摘要:
The present invention provides the in-vitro use of at least one in-vivo-target antigen of Aspergillus fumigatus for selective activation, detection and/or analysis of Aspergillus fumigatus specific CD4 + T cells in a sample comprising cells, wherein said at least one in-vivo-target antigen reveals an immune reactivity characterized by i) the in vivo existence of antigen-specific T cells comprising more than 60% memory T cells and ii) said antigen-specific T cells further comprise T cells able to produce IFN-gamma upon stimulation at a frequency between 15% and 80% and/or IL17 upon stimulation at a frequency between 5% and 30%. Said at least one in-vivo-target antigen may be selected from the group consisting of antigens Scw4, Pst1, Shm2, GliT and TpiA or fragments thereof. Also provided are a method, a composition, and a kit thereof.
摘要:
The present invention provides the in-vitro use of at least one in-vivo-target antigen of Aspergillus fumigatus for selective activation, detection and/or analysis of Aspergillus fumigatus specific CD4 + T cells in a sample comprising cells, wherein said at least one in-vivo-target antigen reveals an immune reactivity characterized by i) the in vivo existence of antigen-specific T cells comprising more than 60% memory T cells and ii) said antigen-specific T cells further comprise T cells able to produce IFN-gamma upon stimulation at a frequency between 15% and 80% and/or IL17 upon stimulation at a frequency between 5% and 30%. Said at least one in-vivo-target antigen may be selected from the group consisting of antigens Scw4, Pst1, Shm2, GliT and TpiA or fragments thereof. Also provided are a method, a composition, and a kit thereof.
摘要:
The invention relates to paramagnetic beads comprising iron oxide and aminodextran having a zeta potential of 5 to 100 mV. The paramagnetic beads can be used for in vivo cell tracking by MRI.
摘要:
Lipophilic oligonucleotide comprising a phosphate glycerol unit containing at least one aliphatic unsaturated carbon bond according to formula I
with Oligonucleotide = an unmodified or modified nucleic acid of 2 - 1000 nucleotides in length R = a bond or a linker unit Y = OH, SH or NHR3 X and Z = independently O, S or NR3 R3 = hydrogen or branched or unbranched and/or substituted or unsubstituted alkyl, aryl and/or alkyl aryl residue with 10 to 30 carbon atoms R1, R2 = branched or unbranched and/or substituted or unsubstituted alkyl, aryl and/or alkylaryl residue with 10 to 30 carbon atoms, with the provisio that at least one of the residues R1 or R2 comprises at least one aliphatic carbon-carbon double bond Use of lipophilic oligonucleotide according to Formula I for drug discovery or for transfection of cells.
摘要:
The present invention provides a polynucleotide and a method for screening and enriching a recombinant protein expressed in a eukaryotic cell, the polynucleotide comprising a tricistronic expression cassette comprising a) a promoter, b) a gene of interest (GOI), c) a reporter gene, d) a selection marker gene, e) an internal ribosome entry site (IRES) element, and f) a 2A element. Said method comprises a) transfecting or transducing suitable eukaryotic host cells with the polynucleotides of the present invention, b) culturing the eukaryotic host cells under conditions so as to express the protein of interest, the reporter protein and the selection marker protein in a cell culture selection medium suitable for selecting positively-transfected/transduced cells by means of said selection marker, and c) screening, sorting and/or enriching the cells expressing high levels of protein of interest by means of the reporter protein.
摘要:
The invention is directed to a device for fragmenting or homogenizing biological samples, comprising: - a tubular laboratory test vessel (1) having an open first end (3) and a second end closed by a bottom (10); - a closing lid (2) for the laboratory test vessel (1) connected to the open end (3) of the laboratory test vessel (1); - a processing tool (5) arranged in said closing lid (2), comprising a plurality of teeth (4a-c) and an agitating element (11) having a guidance tube (13) that is rotatably mounted through a central bore in the lid (2) and includes an engagement portion (16) that is adapted to be engaged by a drive motor; wherein at least one outer cutting blade (6) is located at the periphery of the processing tool (5) and a transportation element (8) is arranged at the guidance tube (13) that extends outwardly in a helical shape over the outer cutting blade (6) and which is provided with slots (6a) fitting the outer cutting blades (6). Furthermore, the invention is directed to a process for extracting, fragmenting, mixing or homogenizing biological samples in a device according to any of the claims 1 to 12 wherein the agitating element (11) is rotated relative to the closing lid (2) and the processing tool (5), thereby guiding the transportation element (8) over at least one group of teeth (4 a-c) and at least one outer cutting blade (6) through slots (6a) of the transportation element (8) in a grinding and cutting manner.
摘要:
The invention relates to a device (1) for removing biological material from an organism. The device (1) comprises: a removal means (2) for removing biological material from an organism, having a bypass means (3) for the selective lumen connection of the removal means (2) to a) a penetration means (6) for penetration into the organism, b) a receiving means (4) for receiving the material from the organism, and c) a storage means (12) for storing a substance. The bypass means (3) is designed such that the removal means (2) can be connected in a lumen manner to the storage means (12) and the receiving means (4), or to the penetration means (6).
摘要:
The invention relates to a system, comprising: a) a sample processing unit, comprising an input port and an output port coupled to a rotating container having at least one sample chamber, the sample processing unit configured provide a first processing step to a sample or to rotate the container so as to apply a centrifugal force to a sample deposited in the chamber and separate at least a first component and a second component of the deposited sample; and b) a sample separation unit coupled to the output port of the sample processing unit, the cell separation unit comprising separation column holder, a pump and a plurality of valves configured to at least partially control fluid flow through a fluid circuitry and a separation column positioned in the holder, the separation column configured to separate labeled and unlabeled components of sample flowed through the column.