Product Name	F(ab')₂ Fragment Goat Anti-Mouse IgG H&L / HRP
Chinese Name	HRP标记的F(ab)2片段羊抗小鼠IgG H&L
Alias	F(ab)2 Fragment Goat Anti-Mouse IgG H&L (HRP); F(ab)2 Fragment Goat Anti-Mouse IgG H&L/HRP; F(ab)2 Fragment Goat Anti-Mouse IgG(H+L);
Immunogen Species	Goat
Clonality	Polyclonal
React Species	Mouse,
Applications	IHC-P=1:1000  not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
Form	Liquid
Concentration	1.0 mg/ml
immunogen	Native Mouse IgG
Lsotype	IgG
Purification	affinity purified by Protein G
Buffer Solution	10 mM TBS (pH=7.4) with 1% BSA, 0.03% Proclin300 and 50% glycerol.
Storage	Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Product Detail	Immunoglobulin G (IgG), is one of the most abundant proteins in serum with normal levels between 8-17 mg/mL in adult blood. IgG is important for our defence against microorganisms and the molecules are produced by B lymphocytes as a part of our adaptive immune response. The IgG molecule has two separate functions; to bind to the pathogen that elicited the response and to recruit other cells and molecules to destroy the antigen. The variability of the IgG pool is generated by somatic recombination and the number of specificities in an individual at a given time point is estimated to be 1011 variants.
Product Picture	Paraformaldehyde-fixed, paraffin embedded (rat pancreas); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (GLP-1(1G9)) Monoclonal Antibody, Unconjugated (SLM-0933M) at 1:200 overnight at 4°C， An HRP-conjugated secondary (SL60296G-HRP, 1:300 dilution) was used for 20min at 37℃，DAB was used as the chromogen。 Paraformaldehyde-fixed, paraffin embedded (rat cerebellum); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (S100B) Monoclonal Antibody, Unconjugated (SLM-10832M) at 1:200 overnight at 4°C， An HRP-conjugated secondary (SL60296G-HRP, 1:300 dilution) was used for 20min at 37℃，DAB was used as the chromogen。

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