Anti-GFP antibody is a goat polyclonal antibody that is used to detect GFP in ELISA, ICC/IF, IF, IHC-Fr, IHC-FrFl, IHC-P, IP, Western blot.
- Tried and trusted by researchers since 2001
pH: 7.2
Preservative: 0.01% Sodium azide
Constituents: 0.88% Sodium chloride, 0.424% Potassium phosphate solution
IP | ELISA | WB | IF | IHC-P | ICC/IF | IHC-Fr | IHC-FrFl | |
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Tag | Expected | Expected | Tested | Tested | Tested | Tested | Tested | Tested |
Species | Dilution info | Notes |
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Species Tag | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Tag | Dilution info 1/10000.00000 - 1/30000.00000 | Notes This antibody 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. |
Species | Dilution info | Notes |
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Species Tag | Dilution info 1/400.00000 - 1/2000.00000 | Notes (for immunoprecipitated GFP, see Abreview). |
Species | Dilution info | Notes |
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Species Tag | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Tag | Dilution info 1/200.00000 - 1/1000.00000 | Notes - |
Species | Dilution info | Notes |
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Species Tag | Dilution info 1/500 | Notes - |
Species | Dilution info | Notes |
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Species Tag | Dilution info 1/200.00000 - 1/1000.00000 | Notes - |
Species | Dilution info | Notes |
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Species Tag | Dilution info - | Notes - |
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Energy-transfer acceptor. Its role is to transduce the blue chemiluminescence of the protein aequorin into green fluorescent light by energy transfer. Fluoresces in vivo upon receiving energy from the Ca(2+)-activated photoprotein aequorin.
Green fluorescent protein, GFP
Anti-GFP antibody is a goat polyclonal antibody that is used to detect GFP in ELISA, ICC/IF, IF, IHC-Fr, IHC-FrFl, IHC-P, IP, Western blot.
- Tried and trusted by researchers since 2001
pH: 7.2
Preservative: 0.01% Sodium azide
Constituents: 0.88% Sodium chloride, 0.424% Potassium phosphate solution
No reaction was observed against Human, Mouse or Rat serum proteins.
This anti-GFP antibody cross reacts with eGFP .
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.
Anti-GFP antibody (ab6673) was first used in a scientific publication in 2005 and has been cited over 544 times in peer reviewed journals. It's performance in IHC, immunofluorescence and Western Blot is trusted by the scientific community.
Abcam's high quality validation processes ensure Anti-GFP antibody (ab6673) has high sensitivity and specificity.
Anti-GFP antibody (ab6673) has 11 independent reviews from customers.
GFP antibodies are used to visualize proteins labelled with this tag in a variety of applications (for example imaging and Flow cytometry). To enable specific detection of your tagged protein, Anti-GFP antibody (ab6673) has been validated in ELISA, ICC/IF, IF, IHC-Fr, IHC-FrFl, IHC-P, IP and WB.
Anti-GFP antibody (ab6673) specifically detects GFP (UniProt ID: P42212; Molecular weight: 27kDa) and is sold in 100 µg selling sizes.
Green Fluorescent Protein (GFP), originally derived from the jellyfish Aequorea victoria, emits a bright green fluorescence under ultraviolet or blue light. This unique property makes GFP an invaluable tool in molecular and cell biology research. Widely used to tag proteins, GFP allows scientists to visualize and track protein expression, localization and interactions within living cells. Key applications of GFP include fluorescence microscopy (ICC, IHC, IF), flow cytometry (FC) and western blotting (WB).
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Full details and terms and conditions can be found here:
Terms & Conditions.
Immunofluorescence of TGN mouse liver labeling GFP on hepatocytes with ab6673.
Pth4:eGFP transgenic zebrafish embryos at 1 and 2 dpf were fixed with 4% PFA and washed in PBST. They were then washed in PBDT (1% BSA, 1% DMSO, 0.1% Triton X-100 in PBS, pH 7.4), blocked in 10% normal goat serum/PBDT, and incubated overnight at 4°C with primary antibodies to HuC/D (1/100) and GFP (1/400, Abcam ab6673). Further PBST washes and blocking were followed by secondary antibodies overnight at 4°C. Hoechst 34580 was added to stain nuclei (1/2500). After further PBDT and PBS washes, embryos were mounted for confocal imaging.
Abbreviation: e, eye; hy, hypothalamus; m, midbrain; sc, spinal cord. Scale bars: 100 μm (A-C) 50 μm (D-G).
(Panels D-E") Expression of the constructs was assessed.
(Panels D-D'') 2 days after transfection in vitro.
(Panels E-E'') at P21 in vivo.
Immunochemistry for FLAG and GFP showed that constructs encoding either WT Disc1, the Disc1-100P variant, or GFP alone, expressed these protein species in transfected HEK-293 cells in vitro (Fig 5D–5D") and in P21 postmitotic cortical neurons in vivo (Fig 5E–5E")
VML affected muscle from the 50% MG + HA+LMN group were probed for the presence of GFP. GFP+ fibers were detected in a qualitatively similar magnitude at both 2 and 8 weeks post-injury indicating viable engraftment of donor derived muscle progenitor cells. Scale bars are 1mm for whole mount images, 50 μm for regions of interest.
A portion of the TA muscle from the defect region was embedded in a talcum-based gel, frozen in 2-methylbutane, and supercooled in liquid nitrogen. Cryosections (8 μm) were prepared and stained using standard protocols for hematoxylin & eosin.
ab6673 used at a 1/100 dilution.
Mouse small intestines were washed with DPBS and fixed overnight at 4°C in Zinc formalin. Following sectioning and tissue deparaffanization, antigen retrieval was performed with 10mM Tris base (pH 9.0) buffer using a pressure cooker.
For immunohistochemistry, sections were quenched of endogenous peroxidases by 3% H2O2, and sequentially blocked with Avidin D, biotin, and protein blocking reagents. Primary antibody incubation was conducted at 4°C overnight. Secondary biotinylated antibody was added at a dilution of 1/200, and incubated 2 hours at room temperature. Finally, sections were stained according to the ABC peroxidase protocol and counterstained with hematoxylin.
ab6673 used at a 1/200 dilution.
Panel D: Representative anti-eGFP immunofluorescence of macroH2A WT and DKO jejunum counterstained with DAPI (blue).
Blocking Buffer: 1% Casein-TTBS for 30 min at RT.
All lanes: Western blot - Anti-GFP antibody (ab6673) at 1 µg/mL
Lane 1: HEK-293 (Human epithelial cell line from embryonic kidney) lysate at 10 µg
Lane 2: HeLa (Human epithelial cell line from cervix adenocarcinoma) lysate at 10 µg
Lane 3: CHO/K1 lysate at 10 µg
Lane 4: MDA-MB-231 (Human breast adenocarcinoma cell line) lysate at 10 µg
Lane 5: A431 (Human epidermoid carcinoma cell line) lysate at 10 µg
Lane 6: Jurkat (Human T cell leukemia cell line from peripheral blood) lysate at 10 µg
Lane 7: NIH/3T3 (Mouse embryo fibroblast cell line) lysate
Lane 8: E-coli HCP control, 50 ng
Lane 9: FLAG Positive control lysate at 10 µg
Lane 10: Red fluorescent protein, 50 ng
Lane 11: Green fluorescent protein, 50 ng
Lane 12: Glutathinoe-S-Transferase protein, 50 ng
Lane 13: Maltose Binding protein, 50 ng
All lanes: Peroxidase goat secondary antibody, 60 min at RT at 1/30000 dilution
Predicted band size: 27 kDa
Tissue: Drosophila melanogaster late stage embryonic central nervous system.
Fixation: 0.5% PFA.
Antigen retrieval: Not required.
Primary antibody: Anti-GFP antibody at a 1/1,000 for 1 h at RT.
Secondary antibody: AlexaFluor 488™ conjugated anti-Goat antibody at 1/300 for 45 minutes at RT.
Panel A: shows a lateral view (ventral left).
Panels B and C: shows ventral views of whole mount embryos at 63x magnification (plus 2x digital zoom).
In all panels, anterior is up.
Staining: tau-GFP cell bodies (large arrowhead) and axons of motorneurons (arrow) and interneurons (small arrowhead) as green fluorescent signal.
E5.5 Hex-GFP transgenic mouse embryo stained for GFP using ab6673 at 1/500 dilution. Secondary antibody is a fluorochrome conjugated anti-goat IgG secondary antibody at 1/10,000 for 45 min at RT.
Staining: GFP as green fluorescent signal with DAPI blue counterstain.
All lanes: Western blot - Anti-GFP antibody (ab6673) at 1 µg/mL
Lane 1: HeLa (Human epithelial cell line from cervix adenocarcinoma) cells at 35 µg
Lane 2: Mock transfected HeLa cell lysate at 35 µg
All lanes: IRDye® 800 conjugated Donkey-a-Goat IgG [H&L] at 1/2500 dilution
Predicted band size: 27 kDa
Observed band size: 33 kDa
All lanes: Western blot - Anti-GFP antibody (ab6673) at 1/1000 dilution
Lane 1: MRC5VA lung fibroblast whole cell lysate overexpressing EGFP alone at 15 µg
Lanes 2 - 3: MRC5VA lung fibroblast whole cell lysate overexpressing an EGFP fusion protein at 15 µg
All lanes: HRP-conjugated anti-goat polyclonal at 1/10000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 27 kDa
Observed band size: 27 kDa, 55 kDa
Exposure time: 5s
Immunohistochemistry of GFP transgenic mouse liver labeling GFP with ab6673.
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