Goat Anti-Canine IgG(H+L)-HRP



Datasheet      Tech Support









Antibody Testing Data:

ELISA plate was coated with purified canine IgG. Immunoglobulin was detected with Goat Anti-Canine IgG(H+L)-HRP (SB Cat. No. 6070-05).








Product Details






Product Specifications

Name:

Goat Anti-Canine IgG(H+L)-HRP

Clone:

-

Isotype:

Goat IgG (Isotype Control:Goat IgG-FITC)

Specificity:

Reacts with the heavy and light chains of canine IgG

Format/Conjugate:

HRP (Horseradish Peroxidase)

Buffer Formulation:

50% Glycerol/50% Phosphate buffered saline, pH 7.4

Concentration:

-

Volume:

1.0 mL

Storage & Handling:

2-8°C blue Please refer to product specific SDS.

RRID:

AB_2796147

Recommended Dilutions:

Please refer to product specific Technical Guide.

Applications:

Quality tested applications for relevant formats include -
ELISA 1,2
FLISA
Other referenced applications for relevant formats include -
Immunohistochemistry-Frozen Sections 3
Immunocytochemistry 4
Western Blot 5-8

More information:

Source: Pooled antisera from goats hyperimmunized with bovine IgG,

Cross Adsorption: None; may react with immunoglobulins from other species and the light chains of other bovine immunoglobulins, Purification: Affinity chromatography on bovine IgG covalently linked to agarose

Purification: Affinity chromatography on canine IgG covalently linked to agarose

*For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
















References






1. Kakkis E, Lester T, Yang R, Tanaka C, Anand V, Lemontt J, et al. Successful induction of immune tolerance to enzyme replacement therapy in canine mucopolysaccharidosis I. Proc Natl Acad Sci USA. 2004;101:829-34. (ELISA)

2. Dickson P, Peinovich M, McEntee M, Lester T, Le S, Krieger A, et al. Immune tolerance improves the efficacy of enzyme replacement therapy in canine mucopolysaccharidosis I. J Clin Invest. 2008;118:2868-76. (ELISA)

3. Wiberg ME, Saari SA, Westermarck E, Meri S. Cellular and humoral immune responses in atrophic lymphocytic pancreatitis in German shepherd dogs and rough-coated collies. Vet Immunol Immunopathol. 2000;76:103-15. (IHC-FS)

4. Ulchar I, Celeska I, Stefanovska J, Jakimovska A. Hematological and biochemical parameters in symptomatic and asymptomatic leishmania-seropositive dogs. Mac Vet Rev. 2015;38:i-viii. (ICC)

5. Mathis A, Åkerstedt J, Tharaldsen J, Ødegaard Ø, Deplazes P. Isolates of Encephalitozoon cuniculi from farmed blue foxes (Alopex lagopus) from Norway differ from isolates from Swiss domestic rabbits (Oryctolagus cuniculus). Parasitol Res. 1996;82:727-30. (WB)

6. Rasmussen UB, Benchaibi M, Meyer V, Schlesinger Y, Schughart K. Novel human gene transfer vectors: evaluation of wild-type and recombinant animal adenoviruses in human-derived cells. Hum Gene Ther. 1999;10:2587-99. (WB)

7. Müller-Doblies UU, Herzog K, Tanner I, Mathis A, Deplazes P. First isolation and characterisation of Encephalitozoon cuniculi from a free-ranging rat (Rattus norvegicus). Vet Parasitol. 2002;107:279-85. (WB)

8. Burk SV. Detection of antibodies against Parascaris equorum excretory-secretory antigens [dissertation]. Lexington (USA): University of Kentucky, 2013 (WB)










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