HSP90 Antibody (AC88) - BSA Free

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972]

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972] - Analysis using the DyLight 488 conjugate of NB100-1972. Staining of 106 Jurkat cells using HSP90 mAb (AC88), DyLight 488 Conjugate at a concentration of 50ug/ml.

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972]

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972] - Analysis using the Alexa Fluor 405 conjugated HSP90 antibody, NB100-1972AF405 (purple) and fluorescence minus one control (orange). Staining of HSP90 in Primary CD4+ T-cells derived from human peripheral blood using 1uL of antibody per 1X10e5 cells. Image from verified customer review.

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972]

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972] - Analysis using the PE conjugate of NB100-1972. Staining of 10^6 Jurkat cells using HSP90 mAb (AC88), R-Phycoerythrin Conjugate at a concentration of 10ug/mL

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972]

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972] - An intracellular stain was performed on HeLa cells with HSP90 Antibody (AC88) NB100-1972AF647 (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 2.5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 647.

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972]

Flow Cytometry: HSP90 Antibody (AC88) [NB100-1972] - An intracellular stain was performed on Jurkat cells with HSP90 Antibody (AC88) NB100-1972AF647 (blue) and a matched isotype control (orange). Cells were fixed with 4% PFA and then permeabilized with 0.1% saponin. Cells were incubated in an antibody dilution of 5 ug/mL for 30 minutes at room temperature. Both antibodies were conjugated to Alexa Fluor 647.

Western Blot: HSP90 Antibody (AC88) - BSA Free [NB100-1972] -

MAPK8, CDK10, and GSK3 beta are associated with exosomes: (A) Schematic diagram of the differential ultracentrifugation and size exclusion chromatography exosome isolation methods. (B) U1 exosomes and (C) ACH2 exosomes isolated via differential ultracentrifugation are loaded onto IZON 35 nm qEV original exclusion columns. Forty fractions are collected and pooled in sets of 5. Pooled fractions are then probed for MAPK8, CDK10, GSK3 beta, HSP90, and CD63 using Western blot. This figure is representative of a data set of n = 1. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/39851547), licensed under a CC-BY license. Not internally tested by Novus Biologicals.