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Goat Anti-Mouse IgG2b, Fc gamma Specific Antibody (HRP Conjugate) #43593

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  • WB
Western Blotting Image 1: Goat Anti-Mouse IgG2b, Fc gamma Specific Antibody (HRP Conjugate)
Western blot analysis of mouse IgG subclasses (10 ng per lane) reduced and denatured in 1x SDS loading buffer with DTT using Goat Anti-Mouse IgG2b, Fc gamma Specific Antibody (HRP Conjugate) (left) or Anti-mouse IgG, HRP-linked Antibody #7076 (right).
1/1

To Purchase # 43593

Supporting Data

REACTIVITY M
SENSITIVITY
MW (kDa)
Source/Isotype Goat
Application Key:
  • WB-Western Blotting 
Species Cross-Reactivity Key:
  • M-Mouse 
  • Related Products

Product Information

Product Description

Affinity purified Goat Anti-Mouse IgG2b, Fc gamma Specific antibody is conjugated to horseradish peroxidase (HRP). This product has been optimized for use as a secondary antibody in Western blotting applications.

Product Usage Information

Recommended Antibody Dilutions:

1:3000 - 1:5000

Recommended antibody dilutions are provided in ranges because the optimal dilution is dependent on many factors, such as antigen density and permeability.

Storage

Supplied in 0.01M Sodium Phosphate, 0.25M NaCl, pH 7.6, 15 mg/ml Bovine Serum Albumin (IgG-Free, Protease- Free) and 50% glycerol. Store at –20°C. Do not aliquot the antibody.

Protocol

Specificity / Sensitivity

Goat Anti-Mouse IgG2b, Fc gamma Specific Antibody (HRP Conjugate) detects the Fc portion of mouse IgG2b but does not cross-react with other mouse IgG subclasses, mouse IgM, or the Fab portion of mouse immunoglobulins. This antibody has minimal cross-reaction with human, bovine, and rabbit serum proteins. It may cross-react with immunoglobulins from other species.

Species Reactivity:

Mouse

Source / Purification

Goat Anti-Mouse IgG2b, Fc gamma Specific Antibody (HRP Conjugate) is produced by immunizing goats with mouse IgG2b. The Anti-Mouse IgG2b, Fc gamma Specific Antibody is purified from antisera by immunoaffinity chromatography using antigens coupled to agarose beads.

Background

Chemiluminescence systems have emerged as the best all-around method for western blot detection. They eliminate the hazards associated with radioactive materials and toxic chromogenic substrates. The speed and sensitivity of these methods are unequalled by traditional alternatives, and because results are generated on film, it is possible to record and store data permanently. Blots detected with chemiluminescent methods are easily stripped for subsequent reprobing with additional antibodies. HRP-conjugated secondary antibodies are utilized in conjunction with specific chemiluminescent substrates to generate the light signal. HRP conjugates have a very high turnover rate, yielding good sensitivity with short reaction times.

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    For Research Use Only. Not For Use In Diagnostic Procedures.
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