Recombinant A. victoria GFP protein is a Aequorea victoria Full Length protein, in the 1 to 238 aa range with >95% purity, < 1 EU/µg endotoxin level and suitable for western blot, Functional studies and SDS-PAGE. The predicted molecular weight of ab84191 recombinant protein is 26.8 kDa.
- Save time and ensure accurate results - use our recombinant GFP protein as a control
- Available in different sizes to fit your experimental needs
M S K G E E L F T G V V P I L V E L D G D V N G H K F S V S G E G E G D A T Y G K L T L K F I C T T G K L P V P W P T L V T T F S Y G V Q C F S R Y P D H M K Q H D F F K S A M P E G Y V Q E R T I F F K D D G N Y K T R A E V K F E G D T L V N R I E L K G I D F K E D G N I L G H K L E Y N Y N S H N V Y I M A D K Q K N G I K V N F K I R H N I E D G S V Q L A D H Y Q Q N T P I G D G P V L L P D N H Y L S T Q S A L S K D P N E K R D H M V L L E F V T A A G I T H G M D E L Y K
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application SDS-PAGE | Reactivity Reacts | Dilution info - | Notes - |
Application WB | Reactivity Reacts | Dilution info - | Notes ab84191 can be used as a WB positive control in conjunction with Anti-GFP antibody ab290. |
Application FuncS | Reactivity Reacts | 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
Recombinant A. victoria GFP protein is a Aequorea victoria Full Length protein, in the 1 to 238 aa range with >95% purity, < 1 EU/µg endotoxin level and suitable for western blot, Functional studies and SDS-PAGE. The predicted molecular weight of ab84191 recombinant protein is 26.8 kDa.
- Save time and ensure accurate results - use our recombinant GFP protein as a control
- Available in different sizes to fit your experimental needs
pH: 8
Constituents: 10% Glycerol (glycerin, glycerine), 0.316% Tris HCl
Purified using conventional chromatography techniques.
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.
Belongs to the GFP family.
Contains a chromophore consisting of modified amino acid residues. The chromophore is formed by autocatalytic backbone condensation between Ser-65 and Gly-67, and oxidation of Tyr-66 to didehydrotyrosine. Maturation of the chromophore requires nothing other than molecular oxygen.
This product is an active protein and may elicit a biological response in vivo, handle with caution.
Ensure the validity of your result using our Recombinant A. victoria GFP protein ab84191 as a control. ab84191 can be used as a positive control in SDS-PAGE and western blot assays.
Check out our Western blot protocol for more information here
Endotoxin Level determined by LAL method.
Concentration determined by Bradford assay.
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Full details and terms and conditions can be found here:
Terms & Conditions.
**Block:** Blocking buffer for 30 minutes at RT.
All lanes: Western blot - FITC Anti-GFP antibody (FITC Anti-GFP antibody ab6662)
All lanes: Western blot - Recombinant A. victoria GFP protein (ab84191)
All lanes: Fluorescein goat secondary antibody for 60 minutes at RT at 1/1000 dilution
Predicted band size: 27 kDa
Secondary antibody - goat anti-rabbit HRP preadsorbed (Goat Anti-Rabbit IgG H&L (HRP) preadsorbed ab97080)
All lanes: Western blot - Anti-GFP antibody (Anti-GFP antibody ab290) at 1/2500 dilution
All lanes: Western blot - Recombinant A. victoria GFP protein (ab84191) at 0.01 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) preadsorbed (Goat Anti-Rabbit IgG H&L (HRP) preadsorbed ab97080) at 1/5000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 27 kDa
Observed band size: 27 kDa
Exposure time: 30s
This blot was produced using a 4-12% Bis-tris gel under the MES buffer system. The gel was run at 200V for 35 minutes before being transferred onto a Nitrocellulose membrane at 30V for 70 minutes. The membrane was then blocked for an hour using 3% milk before being incubated with HRP Anti-GFP antibody [E385] ab190584 overnight at 4°C. Antibody binding was visualised using ECL development solution ECL Substrate Kit (High Sensitivity) ab133406.
All lanes: Western blot - HRP Anti-GFP antibody [E385] (HRP Anti-GFP antibody [E385] ab190584) at 1/10000 dilution
Lane 1: Western blot - Recombinant A. victoria GFP protein (ab84191) at 0.1 µg
Lane 2: Western blot - Recombinant RFP protein (Recombinant RFP protein ab51993) at 0.1 µg
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 27 kDa
Observed band size: 27 kDa
Exposure time: 10s
1. Prepare a 150 μl recombinant GFP with various concentrations (0.00074 nM - 6.21 μM) in assay buffer and equilibrate to 25°C. (Assay buffer: 10 mM Tris-HCl (pH 8.0), 10 mM EDTA, 0.02% sodium azide.)
2. Read at excitation wavelengths 485 nm and emission 535 nm.
- 96 Well Polystyrene Microplate, black
- Fluorescent plate reader
3 ug of reduced ab84191 on SDS-PAGE, stained with Coomassie Blue.
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