R1091TR GFP antibody

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1 mg / €560.00
Please visit the country specific website of OriGene Technologies or contact your local Distributor to buy this product.

Quick Overview

Goat anti GFP

R1091TR

Product Description for GFP

Goat anti GFP.
Presentation: Texas Red
Product is tested for Frozen Sections, Immunocytochemistry/Immunofluorescence.

Properties for GFP

Product Category Primary Antibodies
Target Category
Quantity 1 mg
Synonyms GFP-Tag, Green fluorescent protein
Presentation Texas Red
Applications C, ICC/IF
Clonality Polyclonal
Host Goat
Shipping to Worldwide
PDF datasheet View Datasheet
Manufacturer OriGene Technologies GmbH
Material safety datasheet MSDS for Polyclonal Antibodies (de)

Datasheet Extract

Immunogen
Swiss Prot Num:
P42212
Immunogen:
GST-Green Fluorescent Protein (GFP) fusion protein corresponding to the full length amino acid sequence (246aa) derived from the jellyfish Aequorea victoria.
Application This product is designed for Immunofluorescence microscopy, Fluorescence based plate assays (FLISA) and Fluorescent Western blotting. This product is also suitable for multiplex analysis, including multicolor imaging, utilizing various commercial platforms.
Recommended Dilutions:
FLISA: > 1/20,000.
Western Blot: > 1/10,000.
Immunofluorescence: 1/500-1/2,500.
Note: This GFP antibody is designed to detect GFP and its variants. It 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 Monoclonal GFP antibody (R1461P) 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 (RA021HRP). 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.
Background Green fluorescence protein (GFP) is a 27 kDa protein derived from the jellyfish Aequorea victoria, which emits green light (emission peak at a wavelenth of 509 nm) when excited by blue light (excitation peak at a wavelenth of 395 nm). Green Fluorescent Protein (GFP) has become an invaluable tool in cell biology research, since its intrinsic fluorescence can be visualized in living cells. GFP fluorescence is stable under fixation conditions and suitable for a variety of applications. GFP has been widely used as a reporter for gene expression, enabling researchers to visualize and localize GFP-tagged proteins within living cells without the need for chemical staining. Other applications of GFP include assessment of protein protein interactions through the yeast two hybrid system and measurement of distance between proteins through fluorescence energy transfer (FRET) protocols. GFP technnology has considerably contributed to a greater understanding of cellular physiology.

YFP differs from GFP due to a mutation at T203Y; antibodies raised against full-length GFP should also detect YFP and other variants.
Concentration 1.0 mg/ml (by UV absorbance at 280 nm)
Product Citations
Purchased from Acris:
TRITC conjugated antibody is cited in:
  1. Suzuki Y, Mogami H, Ihara H, Urano T. Unique secretory dynamics of tissue plasminogen activator and its modulation by plasminogen activator inhibitor-1 in vascular endothelial cells. Blood. 2009 Jan 8;113(2):470-8. doi: 10.1182/blood-2008-03-144279. Epub 2008 Oct 15. PubMed PMID: 18922856.
Unconjugated antibody is cited in:
  1. Niv F, Keiner S, Krishna -, Witte OW, Lie DC, Redecker C. Aberrant neurogenesis after stroke: a retroviral cell labeling study. Stroke. 2012 Sep;43(9):2468-75. doi: 10.1161/STROKEAHA.112.660977. Epub 2012 Jun 26. PubMed PMID: 22738919.
General Readings
  1. J.A. Titus, et.al. J. Immunol. Methods 50; 193, 1982. (Conjugation)
Storage Store vial at 2-8°C prior to restoration. Centrifuge product if not completely clear after standing at room temperature. For extended storage aliquot contents and freeze at -20°C or below. This product is stable for one month at 2-8°C as an undiluted liquid.
Dilute only prior to immediate use.
Avoid cycles of freezing and thawing.
Shelf life: One year from despatch.
Format
Label:
(TM) (TR, MW 625 daltons)
Texas Red
Absorption emission:
596 nm / 620 nm
Molar radio:
4.2 moles Texas Red per mole of Goat IgG.
Purification:
Immunoaffinity Chromatography using Green Fluorescent Protein (Aequorea victoria) coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities.
Buffer System:
0.02M Potassium Phosphate, 0.15M Sodium Chloride, pH 7.2 witn 10 mg/ml BSA (IgG and Protease free) as stabilizer and 0.01% (w/v) Sodium Azide as preservative.
Purity:
/
State:
Lyophilized purified Ig fraction.
Reconstitution:
Restore with 1.0 ml of deionized water (or equivalent).
Specificity
Specificity:
Assay by Immunoelectrophoresis resulted in a single precipitin arc against anti-Goat Serum and purified and partially purified Green Fluorescent Protein (Aequorea victoria) Serum.
No reaction was observed against Human, Mouse and Rat Serum Proteins.
FocusOn and Reviews
FocusOns:

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