Does NOT include antibodies, serum, immunoglobulins, immunoglobulin fragments or enzymes.
Additionally obtainable in azide-free for stay cell, useful assays and Stream cytometry. Fc Blocker can be utilized for stay cells and useful assays which might be delicate to sodium azide with none cytotoxicity or cell demise.
Azide-Free Fc Blocker can also be used for Stream cytometry.
Innovex Fc Receptor Block is a peptide primarily based expertise designed to dam Fc Receptors current on all leukocytes (white blood cells), lymphomas, leukemias and melanomas. Fc receptors are additionally expressed on a majority of tumors; Blocking the Fc receptors is important for correct typing of lymphoid and tumor tissues and cells. Fc receptor staining happens by the binding of Fc receptors current on cells to the Fc area of the first and/or secondary antibody and isotype controls. Fc Receptor Block can be utilized for IHC (frozen and paraffin), immunofluorescence, circulation cytometry, and in-situ hybridization. For stay cell and useful assays use of Azide-Free Fc Block is advisable.
Fc Receptor Blocker is a should for correct lymphoma, leukemia and melanoma typing and in addition for Background-free Kappa and lambda staining
INNOVEX BIOSCIENCES Fc Receptor
ADVANCED AND UNIQUE FEATURES
Blocks Fc Receptors in each human and animal cells
30 minute incubation step at room temperature for human tissues/cells
45 minutes to 1-hour incubation for animal tissues/cells
Eliminates false constructive staining of white blood cells, lymphoid tissues, cytosmears (blood & bone marrow), melanoma tumors and different Fc expressing tumors
Insures correct lymphoma and leukemia typing
liminates unfavorable management staining of lymphomas, lymphoid tissues, and blood and bone marrow smears
Eliminates false constructive staining for Kappa and Lambda staining
Eliminates false constructive staining of Reed Sternberg cells
A should for CD markers staining in IHC, immunofluorescence
A should for CD phenotyping by way of circulation cytometry
A should for Immunoglobulins (Igs) staining by way of IHC, circulation cytometry and immunofluorescence
