GFP (Ads. to Hu, Ms, Rt Serum Proteins) Rabbit Polyclonal Antibody
Specifications
| Product Data | |
| Application | ELISA, FC, IF, IHC, IP, WB |
|---|---|
| Recommended Dilution | WB: 1:500 - 1:5,000 IHC: 1:200 - 1:3,000 IF: 1:500 - 1:5,000 FC: User Optimized ELISA: 1:20,000 - 1:120,000 IP: User Optimized |
| Reactivity | eGFP, GFP, rGFP, RS-GFP, S65T-GFP, YFP |
| Antibody Host | Rabbit |
| Isotype | IgG |
| Clonality | Polyclonal |
| Immunogen | The immunogen is a Green Fluorescent Protein (GFP) fusion protein corresponding to the full length amino acid sequence (246aa) derived from the jellyfish Aequorea victoria. |
| Specificity | Anti-GFP antibody was prepared from monospecific antiserum by immunoaffinity chromatography using Green Fluorescent Protein (Aequorea victoria) coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities. Assay by immunoelectrophoresis resulted in a single precipitin arc against anti-Rabbit Serum and purified and partially purified Green Fluorescent Protein (Aequorea victoria). No reaction was observed against Human, Mouse or Rat serum proteins. |
| Buffer | 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2 Stabilizer: None Preservative: 0.01% (w/v) Sodium Azide |
| Concentration | 1.25 mg/mL - lot specific |
| Purification | This product was prepared from monospecific antiserum by immunoaffinity chromatography using Green Fluorescent Protein (Aequorea victoria) coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities |
| Conjugation | Unconjugated |
| Storage | Store Anti-GFP Antibody at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. GFP antibody is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use. |
| Stability | Expiration date is one (1) year from date of receipt. |
| Shipping | Blue Ice |
| Predicted Protein Size | 27 kDa |
| Database Link | |
| Background | Green Fluorescent Protein (GFP) is a 27 kDa protein produced from the jellyfish Aequorea victoria, which emits green light (emission peak at a wavelength of 509nm) when excited by blue light. GFP is an important tool in cell biology research. GFP is widely used enabling researchers to visualize and localize GFP-tagged proteins within living cells without the need for chemical staining. GFP Antibody is ideal for Cell Biology, Neuroscience and Cancer research. |
| Synonyms | rabbit anti-GFP antibody, Green Fluorescent Protein, GFP antibody, Green Fluorescent Protein antibody, EGFP, enhanced Green Fluorescent Protein, Aequorea victoria, Jellyfish |
| Note | Anti-GFP antibody is designed to detect GFP and its variants. GFP antibody has been tested by western blot and ELISA. This product can be used to detect GFP by ELISA (sandwich or capture) for the direct binding of antigen and recognizes wild type, recombinant and enhanced forms of GFP. Biotin conjugated polyclonal anti-GFP used in a sandwich ELISA is well suited to titrate GFP in solution using this antibody in combination with Rockland's monoclonal anti-GFP (600-301-215) using either form of the antibody as the capture or detection antibodies. However, use the monoclonal form only for the detection of wild type or recombinant GFP as this form does not sufficiently detect 'enhanced' GFP. The detection antibody is typically conjugated to biotin and subsequently reacted with streptavidin conjugated HRP (code # S000-03). Fluorochrome conjugated polyclonal anti-GFP can be used to detect GFP by immunofluorescence microscopy in prokaryotic (E.coli) and eukaryotic (CHO cells) expression systems and can detect GFP containing inserts. Significant amplification of signal is achieved using fluorochrome conjugated polyclonal anti-GFP relative to the fluorescence of GFP alone. For immunoblotting use either alkaline phosphatase or peroxidase conjugated polyclonal anti-GFP to detect GFP or GFP containing proteins on western blots. Optimal titers for applications should be determined by the researcher. |
| Reference Data | |
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Citations
Rossi, Helbling-Leclerc, Kawasumi et al
EMBO Rep. (2019) 21 (2), e48222 DOI: 10.15252/embr.201948222
Venters, Cuenca, Hyer
Mol Vis (2011) 17, 3347-63
Schmidt, Bleck, Helenius et al
EMBO J (2011) 30 (17), 3647-61 DOI: 10.1038/emboj.2011.245
Torres, Funk, Zegers et al
J Biol Chem (2011) 286 (12), 10834-46 DOI: 10.1074/jbc.M110.186668
Papadopoulos, Arato, Lilienthal et al
J Biol Chem (2011) 286 (7), 5494-505 DOI: 10.1074/jbc.M110.157909
Kwan, Navarro-Sanchez, Dumortier et al
PLoS Negl Trop Dis (2008) 2 (10), e311 DOI: 10.1371/journal.pntd.0000311
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