Search Results
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描述 Mouse Monoclonal实验应用 ELISA IHC Purification Turbidimetry Sandwich ELISA种属反应 Hu¥4300100 μg
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描述 Mouse Monoclonal实验应用 ELISA IHC Purification Turbidimetry Sandwich ELISA种属反应 Hu¥4300100 μg
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描述 Mouse Monoclonal实验应用 FCM IP ELISA种属反应 Hu, Bov, Primate
Summary This antibody reacts with all human classical MHC Class I molecules (major histocompatibility complex) in native cell-surface forms as well as with human HLA-G cDNA transfected cells. The antibody MEM-123 completely blocks binding of classical W6/32 to surface-expressed HLA-G, but does not cross-blocks the antibody MEM-G/9.
¥4700100 μg -
描述 Mouse Monoclonal实验应用 ELISA IHC Purification Turbidimetry Sandwich ELISA种属反应 Hu¥4300100 μg
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描述 Mouse Monoclonal实验应用 WB IHC-Fr FCM IP种属反应 Chk, Trky¥7000250 μg
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描述 Mouse Monoclonal实验应用 ICC/IF IHC-Fr FCM IP ELISA种属反应 Hu
Summary This antibody recognizes membrane-bound form of HLA-G (full-length HLA-G1), but not soluble forms.
我们不建议将此产品应用于 Mouse,Rat.
¥5000100 μg -
描述 Armenian Hamster Monoclonal实验应用 ICC/IF FCM IP Functional Assay IHC种属反应 Ms¥4700100 μg
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描述 Rat Monoclonal实验应用 WB IHC-Fr FCM IP ELISA Activation种属反应 Ms
Summary The monoclonal antibody HM102 recognizes the extracellular part of membrane-bound TNF-RII as well as the soluble form of TNF-RII which is generated by proteolytic cleavage of the extracellular domain. The soluble form can still bind TNF-alpha with high affinity and functions as a TNF-alpha antagonist. The antibody is a agonistic receptor modulating antibody. It enhances in vitro TNF alpha responses by increasing the affinity of the soluble form of TNF-alpha for TNF-RII.
¥650050 μg -
描述 Mouse Monoclonal实验应用 WB FCM IP种属反应 Hu, ClMK, RMK
Summary The antibody binds to the beta chain, recognising an epitope that is dependent upon expression of both CD8 alpha and CD8 beta.
¥8700200 μg -
描述 Mouse Monoclonal实验应用 WB ICC/IF IHC-P IHC-Fr FCM Functional Assay种属反应 Hu
Summary The CRA1 (AER37) monoclonal antibody reacts with the Fc epsilon R1 alpha subunit on a region that does not overlap the region of the IgE binding site, thus it does not compete withIgE for the receptor binding. Since the CRA2 (AER24) monoclonal antibody reacts with the IgE binding site on Fc epsilon R1 alpha, it competes with IgE for the receptor binding. Combining the two antibodies, one can quantitatively measure the amounts of the IgE-bound Fc epsilon R1 alpha.
¥560050 μg