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Antibodies

Rat IgM (mu chain) Antibody Biotin Conjugated

Product Sizes
1.5 mg
£245.00
612-4607-1.5MG
About this Product
SKU:
612-4607
Additional Names:
Rabbit Anti-Rat IgM (mu chain) Antibody biotin Conjugated, Rabbit Anti-Rat IgM mu Antibody BAC Conjugation
Application:
ELISA, Immunohistochemistry, Microarray, Western Blot
Buffer:
0.02 M Potassium Phosphate, 0.15 M Sodium Chloride
CE/IVD:
RUO
Clonality:
Polyclonal
Conjugate:
Biotin
Concentration:
1.5 mg/ml
Extra Details:
Anti-Rat IgM antibody generated in rabbit specifically detects rat IgM heavy chain. Immunoglobulin M is the largest antibody isotype and the first to be secreted against an initial exposure to antigen. IgM is predominantly produced in the spleen. Formed from covalently linking 5 immunoglobulins together, the approximate molecular weight of IgM is 900kDa and possesses 10 binding sites (though due to the size of most antigens, not all sites are capable of binding at once). Due to this large size, IgM is typically isolated to the serum. Anti-Rat IgM antibody is ideal for investigators in Immunology, Microbiology, and Cell Biology. This Anti-Rat IgM antibody is conjugated to biotin.
Formulation:
0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Host:
Rabbit
Immunogen:
Rat IgM whole molecule
Isotype:
IgG
Physical State:
Lyophilized
Reactivities:
Rat
Shipping Conditions:
Ambient
Specificity:
Anti-RAT IgM (mu chain) Antibody was prepared from monospecific antiserum by immunoaffinity chromatography using Rat IgM coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities. Purified Anti-RAT IgM was Biotin Conjugated. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-biotin, anti-Rabbit Serum, Rat IgM and Rat Serum. No r
Storage Conditions:
2-8[o]C liquid. Aliquot. Avoid freeze/thaw cycles., -20[o]C/-70[o]C aliquoted. Aliquot. Avoid freeze/thaw cycles.
Supplier:
Rockland Inc
Type:
Antibody: Secondary Antibodies
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 150 pg (0.5 mg/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 of Thermotoga maritima; mDectin-1, murine dectin-1; CtCBM11, CBM11 of Clostridium thermocellum; ConA, concanavalin A; AAL, Aleuria aurantia lectin. FIG 2. PMID: 34817219.