Anti-RAT IgM (mu chain) Antibody has been assayed against Rat IgM in a standard capture ELISA using Peroxidase Conjugated Streptavidin. A working dilution of 1:15,000 to 1:70,000 of the concentration is suggested for this product. Rat IgM antibody is sui
Carbohydrate binding by BoSGBPMLG-A using a structurally diverse saccharide microarray. Heatmap comparing the binding patterns of BoSGBPMLG-A and selected control proteins. The microarray comprised soluble saccharides of different origins (fungal, bacterial, plant, and microalgal polysaccharides or glycoproteins) (see Table S1), the major backbone sequences are depicted at the bottom. The heatmap represents the relative binding intensities calculated as the percentage of the fluorescence signal intensity at 150pg (0.5mg/ml)/spot given by the saccharide probe most strongly bound by each protein (normalized as 100%). Results are detailed in Table S2.S. cerevisiae, Saccharomyces cerevisiae,N. oculata,Nanochloropsis oculata,P. palmata,Palmaria palmata,C. albicans,Candida albicans,M. tuberculosis,Mycobacterium tuberculosis,hMalectin, human malectin,TmCBM41, CBM41 ofThermotoga maritima,mDectin-1, murine dectin-1,CtCBM11, CBM11 ofClostridium thermocellum, ConA, concanavalin A, AAL,Aleuria aurantialectin. FIG2. PMID: 34817219.
* VAT and and shipping costs not included. Errors and price changes excepted
