secondary antibody

Goat Anti-Mouse IgG (H+L) Secondary Antibody, FITC Conjugate

BA1101

0.5 ml

Enabled

Goat Anti-Mouse IgG (H+L) Secondary Antibody, FITC Conjugate

Secondary Antibodies, IHC ICC IF Antibodies

0.5ml / $80 1ml / $150

Polyclonal

1mg/ml

FITC

FITC Conjugated Goat Anti-mouse IgG (H+L) secondary antibody This FITC conjugated antibody is specific for mouse IgG and shows no cross-reactivity with human/bovine/rabbit IgG.

This antibody is purified from antiserum by immunoaffinity chromatography which removes essentially all goat serum proteins, except the specific antibody for mouse IgG. The antibody preparation is solid phase adsorbed with human serum proteins to ensure minimal cross reactivity in tissue or cell preparations.

Product Overview Product Name Goat Anti-Mouse IgG (H+L) Secondary Antibody, FITC Conjugate Synonyms FITC-conjugated Goat Anti-mouse IgG; Goat Anti-Mouse IgG-FITC Secondary Antibody; Fluorescein-labeled Goat Anti-Mouse IgG Secondary Antibody;ee Description Goat Anti-Mouse IgG (H+L) Secondary Antibody, FITC Conjugate, for detection, localization and quantification of target proteins in a sample via indirect immunofluorescence in IHC-P, IHC-F, ICC, or FCM Reagent Type Fluorophore-conjugated secondary antibody Label FITC Host Goat Target Species Mouse Antibody Class IgG Clonality Polyclonal Immunogen Whole molecule mouse IgG Purification Immunoaffinity chromatography Solid Phase Adsorbtion Human serum proteins Specificity Mouse IgG specific Form Supplied No cross-reactivity with human/bovine/rabbit IgG Formulation 0.5 mg FITC-conjugated secondary antibody . 0.01 M PBS (PH 7.4) . 0.01% Thimerosal . 50% glycerol Pack Size 0.5 ml Concentration 1 mg/ml Application Flow Cytometry (FCM), Immunohistochemistry (paraffin-embedded (IHC-P) and frozen(IHC-F) sections), Immunocytochemistry (ICC) . *Our Boster Guarantee covers the use of this product in the above marked tested applications. Storage 4C for 1 year Precautions FOR RESEARCH USE ONLY. NOT FOR DIAGNOSTIC OR CLINICAL USE Assay Information Sample Type Cell suspension, FFPE tissue sections, thawed frozen samples Assay Type Immunoanalytical Assay Purpose Protein detection/quantification Technique Immunodetection of target antibody with HRP reporter enzyme Equipment Needed Excitation light source; Filter set and detector: fluorescence microscope (can be combined with confocal microscope), fluorescence plate-reader, flow cytometer, or cell sorter; Main Advantages Specific High signal-to-noise ratio Fast Fewer number of processing steps - no need for adding a substrate; Less optimization required compared to enzymatic detection; Generates strong signals in a relatively short time span; Fluorescence can be observed directly High Signal Amplification Multiple secondary antibodies can bind to a single primary antibody; Multiple FITC molecules bind to a single secondary antibody; High Image Quality High-resolution compatibility with fluorescent microscopy; compatible with multi-planar microscopy Precise target localization Sharp, precise signal development Multiplex Compatibility Colocalization studies: use primary antibodies from different host species for simultaneous detection by fluorophore-conjugated secondary antibodies; use multiple differently colored fluorophores in the same experiment for target differentiation Quantifieable Rapid and precise quantitative analysis of fluorescent signal Background . Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species. The host antiserum is then purified through immunoaffinity chromatography to remove all host serum proteins, except the specific antibody of interest. Purified secondary antibodies are further solid phase adsorbed with other species serum proteins to minimize cross-reactivity in tissue or cell preparations, and are then modified with antibody fragmentation, label conjugation, etc., to generate highly specific reagents. Secondary antibodies can be conjugated to a large number of labels, including enzymes, biotin, and fluorescent dyes/proteins. Here, the antibody provides the specificity to locate the protein of interest, and the label generates a detectable signal. The label of choice depends upon the experimental application. . Immunofluorescence is a technique used for light microscopy with a fluorescence microscope which utilizes fluorescent dyes as reporters. It is being employed in a variety of applications such as cellular imaging and flow cytometry and is commonly used to visualize the distribution of target molecules through a sample, to detect protein location and activation, to identify protein complex formation and conformational changes, to monitor biological processes in vivo. Fluorescent dyes (also known as fluorochromes, fluorophores, or simply fluors) are molecules that can absorb light of a specific energy and wavelength, thereby undergoing excitation, and then re-emit it at a lower energy and longer wavelength upon returning to the ground state.

0.5 ml

Goat

Mouse IgG (whole molecule).

At 4 C for one year.

Flow Cytometry, IHC, ICC

Mouse

PCK was detected in paraffin-embedded sections of human intestinal cancer tissues using mouse anti- PCK Antigen Affinity purified monoclonal antibody (Catalog # MA1081) at 1 ??g/mL. FITC Conjugated Goat Anti-mouse IgG (H+L) secondary antibody (Catalog # BA1101) was used to detect the primary antibody at 30??g/mL.

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