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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다른 시약 추가 (MAP메이트 사용을 위해 완충용액과 검출 키트가 필요함)
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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.
Cells of the innate and adaptive immune system work in concert to protect the body from pathogenic attack. The many different types of immune cells can be distinguished from one another not only by cell surface markers but also by their diverse cellular responses to different pathogens or stimuli. By combining quantitative image analysis tools with the large sample sizes common to flow cytometry, the ImageStream®x uniquely enables multiple applications within the field of Immunology, including measurement of nuclear translocation of transcription factors, T:APC interactions and accumulation of proteins at the immune synapse, chemokine-induced shape change, and phagocytosis, just to name a few.
Ovalbumin-specific accumulation of ADAP at the immune synapse is measured. Without specific peptide ADAP (green) is distributed around the T cell and in the presence of specific peptide ADAP moves to the synapse between the APC and T cell. Quantitation of conjugate formation and representative cells images show that without specific peptide ADAP (green) is distributed around the T cell and in the presence of specific peptide ADAP moves to the synapse between the APC and T cell. See the application note for more details.
NF-kB Translocation in T:APC Conjugates
Measurement of NFκB translocation in transgenic T cells which are in contact with antigen presenting cells (APC) and specific peptide. Specific T cell:APC conjugates are identified and translocation of NFκB from the cytoplasm to the nucleus specifically within the T cells is measured in the presence (shown) or absence of peptide. See the application note for more details.
Phagocytosis by Murine Macrophages
Internalization of zymosan (green) by murine RAW cells (orange) identified by immunophenotyping. Phagocytosis is measured as the percentage of cells with internalized zymosan at 15, 30 and 60 minutes at 37 degrees C.
HIV-Specific Translocation of NFAT
HIV-specific nuclear localization of NFAT was measured in HIV-experienced T cells from peripheral blood of HIV+ patients. HIVgag peptide specifically stimulates NFAT (green) to move to the nucleus (red) in HIV-tetramer positive cells (orange). The Similarity score correlates DRAQ5 nuclear stain with the NFAT signal. The higher the Similarity score, the more translocation is visualized in the example images from each quadrant.
Cells of the innate and adaptive immune system work in concert to protect the body from pathogenic attack. The many different types of immune cells can be distinguished from one another not only by cell surface markers but also by their diverse cellular responses to different pathogens or stimuli. By combining quantitative image analysis tools with the large sample sizes common to flow cytometry, the ImageStream®x uniquely enables multiple applications within the field of Immunology, including measurement of nuclear translocation of transcription factors, T:APC interactions and accumulation of proteins at the immune synapse, chemokine-induced shape change, and phagocytosis, just to name a few.
