Rat IgA HEAVY CHAIN Antibody

Referencia OASA04154

embalaje : 0.25mg

Marca : Aviva Systems Biology

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Datasheets/ManualsPrintable datasheet for Rat IgA HEAVY CHAIN Antibody (OASA04154)
Product Info
Predicted Species ReactivityRat
Product FormatLiquid. Phosphate buffered saline
ClonalityMonoclonal
CloneMARA-1
IsotypeIgG1
HostMouse
ApplicationELISA|IF|IHC-Fr
Additional InformationFusion Partners: Spleen cells from immunised BALB/c mice were fused with cells of the mouse SP2/0 myeloma cell line.
::Preparation: Purified IgG prepared by affinity chromatography
Preservative Stabilisers: 0.09% - Sodium Azide
::Approx Protein Conc: IgG concentration 1 mg/ml
Buffer Solutions: Phosphate buffered saline pH7.4
Reconstitution and Storage-20°C
ImmunogenPurified IR1060 IgA rat myeloma protein.
PurificationPurified IgG prepared by affinity chromatography from tissue culture supernatant
Predicted Homology Based on Immunogen SequenceRat
Concentration1 mg/ml
SpecificityIgA
Application InfoELISA : This antibody may be used as a coating antibody in a sandwich ELISA in combination with clone MARK-1/MARL-15 (OASA0579996P) as detection reagent and purified rat IgA (OPSA10723).
Protocol InformationCitation: 1: Ravindranath RM, Mondino BJ, Adamu SA, Pitchekian-Halabi H, Hasan SA, Glasgow BJ. Immunopathologic features of Staphylococcus aureus endophthalmitis in therat. Invest Ophthalmol Vis Sci. 1995 Nov;36(12):2482-91. PubMed PMID: 7591638.
Species: Rat
Experiment Name: Enzyme-linked immunosorbent assay
Experiment Background: To study the clinical, histopathologic, and immunologic responses to Staphylococcus aureus endophthalmitis in rats
Experimental Steps: Experimental Lewis rats received an intravitreal injection of viable S. aureus (65 organisms), and control rats received sterile saline. The clinical scores, cellular infiltrate, delayed hypersensitivity reaction in skin tests, and serum and vitreous enzyme-linked immunosorbent assay titers of immunoglobulin (Ig) M, IgG, and IgA to ribitol teichoic acid (RTA), the major antigenic determinant of 5. aureus cell wall, were measured and compared on days 3, 7, 10, 14, 21, and 30. The differences were statistically assessed using Mann-Whitney nonparametric <-tests and analysis of variance.
Number Of Protocols: 1
Reference1. Kohler, G. & Milstein, C. (1975) Continuous cultures of fused cells secreting antibody of predefined specificity Nature, 256: 495-497.
2. Schulman, M., Wilde, C.D. & Kohler, G. (1978) A better cell line for making hybridomas secreting specific antibodies Nature, 276: 269-270.
3. Bazin, H., Beckers, A. & Querinjean, P. (1974) Three classes and four (sub)classes of rat immunoglobulins: IgM, IgA, IgE and IgG1, IgG2a, IgG2b, IgG2c Eur.J. Immunol. 4: 44-48.
4. Bazin, H., Beckers, A., Urbain-Vansanten, G., Pauwels, R., Bruyns, C., Tilkin, A.F., Platteau, B. & Urbain, J.J. (1978) Transplantable IgD immunoglobulin-secreting tumors in rat Immunol 121: 2077-2082.
5. Bazin, H., et al. (1984) Rat monoclonal antibodies. II. A rapid and efficient method of purification from ascitic fluid or serum J. Immunol. Methods 71: 9-16.
6. Grabar and Williams (1953) Method permitting the combined study of the electrophoretic and the immunochemical properties of protein mixtures; application to blood serum. Biochem. Biophys. Acta 10: 193.
Protein NameIg alpha-1 chain C region
Description of TargetMOUSE ANTI RAT IgA HEAVY CHAIN
Uniprot IDP01876
Protein Size (# AA)131