Suitable for IHC-Fr, IHC-P, Flow Cyt, IM, ICC/IF, Dot. Preadsorbed to minimise non-specific binding and high background staining. Cited in 9 publications.
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application IHC-Fr | Reactivity Expected | Dilution info - | Notes - |
Application IHC-P | Reactivity Expected | Dilution info - | Notes - |
Application Flow Cyt | Reactivity Expected | Dilution info 1/100 - 1/250 | Notes The maximum amount of reagent required to stain 1 x 106 cells in flow cytometry is approximately 1.0µg of antibody conjugate. Lesser amounts of reagent may be sufficient for staining. |
Application IM | Reactivity Expected | Dilution info - | Notes As a general guideline, dilutions of 1/50 to 1/200 should be suitable for most applications. |
Application ICC/IF | Reactivity Expected | Dilution info 1/100 - 1/250 | Notes - |
Application Dot | Reactivity Reacts | Dilution info - | Notes - |
Ig gamma 1 chain C region, Ig gamma 3 chain C region, Ig gamma 4 chain C region, Ig gamma-2 chain C region, Immunoglobin heavy constant gamma 1, Immunoglobulin G
Suitable for IHC-Fr, IHC-P, Flow Cyt, IM, ICC/IF, Dot. Preadsorbed to minimise non-specific binding and high background staining. Cited in 9 publications.
No reaction was observed against anti-Pepsin, anti-Donkey IgG F(c), Chicken, Guinea Pig, Hamster, Horse, Human, Mouse, Rabbit, or Rat Serum Proteins.
Preservative: 0.01% Sodium azide
Constituents: 1% BSA, 0.88% Sodium chloride, 0.424% Potassium phosphate solution
This product was prepared from monospecific antiserum by immunoaffinity chromatography using Goat IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities, pepsin digestion and chromatographic separation.
Can be used in immunomicroscopy and flow cytometry or FACS analysis as well as other antibody based fluorescent assays requiring extremely low background levels, absence of F(c) mediated binding, lot-to-lot consistency, high titer and specificity.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Very bright secondary antibody and PE is one of the best if you have a weak antigen. I used this in a perfect pairing with FITC in a FACS experiment to check pluripotency markers in human embryonic stem cells.
Antigen: Goat IgG.
Load: 100 ng, 33.3 ng, 11.1 ng, 3.7 ng, or 1.23 ng as indicated.
Secondary antibody: ab7004 at 1:1,000 for 60 min at RT.
Block: Blocking Buffer for Fluorescent Western Blotting for 60 min at RT.
Dot blot analysis of ab7004. Imaged with BioRad ChemiDoc, Rhodamine filter.
All lanes: Dot Blot - Donkey Anti-Goat IgG H&L (PE) preadsorbed (ab7004)
Lane 1: Goat IgG at 100 ng
Lane 2: Goat IgG at 33.3 ng
Lane 3: Goat IgG at 11.1 ng
Lane 4: Goat IgG at 3.7 ng
Lane 5: Goat IgG at 1.23 ng
All lanes: Donkey F(ab')2 Anti-Goat IgG Antibody RPE at 1 µg/mL
Dot blot analysis of ab7004.
All lanes: Dot Blot - Donkey Anti-Goat IgG H&L (PE) preadsorbed (ab7004)
Lane 1: Goat IgG at 100 ng
Lane 2: Goat IgG at 33.3 ng
Lane 3: Goat IgG at 11.1 ng
Lane 4: Goat IgG at 3.7 ng
Lane 5: Goat IgG at 1.23 ng
All lanes: F(ab')2 Donkey anti-Goat IgG Phycoerythrin Conjugated Min X Ch, GP, Ham, Hs, Hu, Ms, Rb, & Rt serum proteins antibody at 1/1000 dilution
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com