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Goat anti mouse igg

Manufactured by MyBioSource
Sourced in United States

Goat anti-mouse IgG is a secondary antibody used in various immunoassays and immunochemical techniques. It is specific for the detection and quantification of mouse immunoglobulin G (IgG).

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2 protocols using goat anti mouse igg

1

Quantitative Detection of E. coli O157:H7

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Mouse monoclonal antibodies to Escherichia coli O157:H7 (MBS568290 and MBS568193) were purchased from Mybiosource (San Diego, CA, USA).
Goat anti-mouse IgG, N-hydroxysuccinimide (NHS), 1-ethyl-3-[3-dimethylaminopropyl]–carbodiimide hydrochloride (EDC), 2-(N-morpholino)ethanesulfonic acid (MES), bovine serum albumin (BSA), phosphate-buffered saline (PBS), silver nitrate (AgNO3), hydroquinone (C6H4-1,4-(OH)2), gold(III) chloride hydrate (HAuCl4), and sodium citrate tribasic dihydrate (C6H5Na3O7·2H2O) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Sodium dodecyl sulfate (SDS) (C12H25NaO4S) was purchased from PanReac AppliChem (Barcelona, Spain).
HS-C2H4-CONH-PEG-C3H6-COOH, MW = 5000 g mol−1 (4900 Da), and CH3O-PEG-NH2, MW = 725–850 Da were purchased from RAPP POLYMER (Tuebingen, Germany). All the reagents were prepared using Milli-Q ultrapure water (resistivity 18.2 MΩ·cm at 25 °C), unless otherwise stated.
An IsoFlow reagent dispensing system (ImageneTechnology, USA) was used to dispense the detection lines (dispense rate 0.100μL mm−1) and the strips were cut with a guillotine Fellowes Gamma (Spain).
A portable strip reader ESE Quant LR3 lateral flow system (Qiagen Inc., Germany) was used to quantify the intensity of the test line by reflectance measurements.
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2

Immunohistochemical Analysis of Immune Cells

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Paraffin blocks were sectioned and transferred to glass microscope slides pre-coated with poly-L-lysine. Slides were dewaxed and rehydrated. Endogenous peroxidase was blocked with 0.3% H 2 O 2 in PBS and nonspecific binding sites were blocked with 1.5% normal rabbit serum in PBS. Sections were incubated with primary mouse anti-rat CD4 (Nova Biologics, INC., USA), mouse anti-rat CD8 (Bio-Rad, USA), rabbit polyclonal anti-mouse phospho-RELA (S536) antibody (phospho-NF-κB-p65) (Cusabio, Bioteck Co, Ltd) or goat anti-rat IgG (ProSci, incorporated, USA) monoclonal antibodies diluted in PBS containing 2% fetal bovine serum in a humid chamber overnight at 4°C. The sections were washed in PBS and incubated with a secondary biotinylated goat anti-mouse IgG (MyBioSource, USA), goat anti-rabbit IgG (Abcam, USA), or biotinylated donkey anti-goat IgG (Bio-Rad, USA) antibodies for 45 min. The slides were subsequently stained for three minutes with a 3-minute diaminobenzidine solution and counterstained in Mayer's hematoxylin solution (Merck, Germany). Slides were evaluated and the positivity for the all immunological markers was identified by a digital camera (Microscope Digital Camera DP70, Tokyo).
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