다음 MAP메이트™는 통합될 수 없습니다: -다른 분석 완충용액이 필요한 MAP메이트™. -인산 특이성 및 총 MAP메이트™ 조합, 예: 총 GSK3β 및 GSK3β(Ser 9). -PanTyr 및 자리 특이성 MAP메이트™, 예: Phospho-EGF 수용체 및 phospho-STAT1(Tyr701). -단일 표적(Akt, STAT3)를 위한 1개 이상의 1 phospho-MAP메이트™. - GAPDH 및 β-Tubulin은 panTyr를 포함하는 키트 또는 MAP메이트™와 통합될 수 없습니다.
Custom Premix Selecting "Custom Premix" option means that all of the beads you have chosen will be premixed in manufacturing before the kit is sent to you.
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96-Well Plate
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48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
공간 절약 옵션 다수의 키트를 구매하시는 고객은 고용량 저장을 위해 키트 포장을 제거하고 비닐백에 담긴 멀티플레스 분석 구성품을 받아 저장 공간을 절약하도록 선택할 수 있습니다.
이 제품은 즐겨찾기에 저장되었습니다.
해당 제품은 고객님의 카트에 추가되었습니다.
이제 다른 키트를 사용자 지정하거나, 사전 혼합된 키트를 선택하거나, 결재하거나 또는 주문 도구를 종료할 수 있습니다.
The field of Oncology is largely concerned with elucidating how cancers develop and how best to develop therapies to treat them. Oncologists commonly employ microscopy not only to identify and classify cancer cells, but also to identify the fragmented nuclei of apoptotic cells treated with a chemotherapeutic drug, or to visualize the binding and subsequent internalization and trafficking of therapeutic monoclonal antibodies. Amnis® imaging flow cytometry is ideally suited to these types of studies, and gives the added benefit of combining immunophenotyping with quantitative morphometric measurements that can be applied to identifying rare sub-populations of potentially metastatic cells, including circulating tumor cells (CTC).
Co-Localization of an Antibody-Drug Conjugate to Endosomes or Lysosomes
In this experiment we use the capabilities of the Imagestream®x system to measure the transit of a fluorescently labeled antibody-drug conjugate (ADC) through the cellular endocytic pathway. The high spatial resolution afforded by the Imagestream®x system allowed accurate measurement of ADC co-localization to endosomes and lysosomes. See the application note for more details.
Apoptotic Index Using the ImageStream
DNA condensation and fragmentation are hallmarks of apoptosis. By measuring the area and the intensities of the brightest portions of the nuclear image, the bright, punctate nuclear imagery of apoptotic cells can be distinguished from the evenly stained nuclear imagery of a normal, healthy nucleus. This makes possible the automated identification of apoptotic cells. When cells begin to dye by apoptosis there is fragmentation and condensation of the DNA. By measuring the area and the intensities of the brightest portions of the nuclear image, the bright, punctate nuclear imagery of apoptotic cells can be distinguished from the evenly stained nuclear imagery of a normal, healthy nucleus. This makes possible the automated identification of apoptotic nuclear morphology. See the application note for more details.
The field of Oncology is largely concerned with elucidating how cancers develop and how best to develop therapies to treat them. Oncologists commonly employ microscopy not only to identify and classify cancer cells, but also to identify the fragmented nuclei of apoptotic cells treated with a chemotherapeutic drug, or to visualize the binding and subsequent internalization and trafficking of therapeutic monoclonal antibodies. Amnis® imaging flow cytometry is ideally suited to these types of studies, and gives the added benefit of combining immunophenotyping with quantitative morphometric measurements that can be applied to identifying rare sub-populations of potentially metastatic cells, including circulating tumor cells (CTC).
