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GFP anticorps

Cet anticorps anti-GFP est un anticorps Souris Monoclonal détectant GFP dans WB, ELISA, IHC, IP, FM, FACS et DB. Adapté pour Aequorea victoria. Ce Primary Antibody a été cité dans 17+ publications.
Rockland
N° du produit ABIN129564
N° du produit (Fournisseur): 600-301-215

Aperçu rapide pour GFP anticorps (ABIN129564)

Antigène

Voir toutes GFP Anticorps
GFP (Green Fluorescent Protein (GFP))

Reactivité

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Aequorea victoria

Hôte

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Souris

Clonalité

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Monoclonal

Conjugué

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Cet anticorp GFP est non-conjugé

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunoprecipitation (IP), Fluorescence Microscopy (FM), Flow Cytometry (FACS), Dot Blot (DB)

Clone

9F9-F9
  • N° du produit (Fournisseur)

    600-301-215

    Fournisseur

    Rockland

    Fonction

    GFP Monoclonal Antibody

    Réactivité croisée (Details)

    Assay by Immunoelectrophoresis resulted in a single precipitin arc against anti-Mouse Serum.

    Attributs du produit

    Synonyms: mouse anti-GFP antibody, Green Fluorescent Protein, GFP antibody, Green Fluorescent Protein antibody, EGFP, enhanced Green Fluorescent Protein, Aequorea victoria, Jellyfish

    Purification

    GFP Monoclonal Antibody was prepared from tissue culture supernatant by Protein A affinity chromatography.

    Stérilité

    Sterile filtered

    Immunogène

    Immunogen: Recombinant Green Fluorescent Protein (GFP) fusion protein corresponding to the full length amino acid sequence (246 aa) derived from the jellyfish Aequorea victoria.

    Immunogen Type: Recombinant Protein

    Isotype

    IgG1 kappa
  • Indications d'application

    Flow Cytometry Dilution: User Optimized

    Immunohistochemistry Dilution: 1:1,000 - 1:5,000

    Application Note: Monoclonal anti-GFP is designed to detect enhanced GFP and GFP containing recombinant proteins. Tested in ELISA, IP, and WB and suitable in FACS, IHC, IF. This antibody can be used to detect GFP by ELISA (sandwich or capture) for the direct binding of antigen. Biotin conjugated monoclonal anti-GFP is well suited to titrate GFP in a sandwich ELISA in combination with Rockland's polyclonal anti-GFP (600-101-215) as the capture antibody. Only use the monoclonal form for the detection of enhanced or recombinant GFP. Polyclonal anti-GFP detects all variants of GFP tested to date. The biotin conjugated detection antibody is typically used with streptavidin conjugated HRP (code # S000-03) or other streptavidin conjugates. The use of polyclonal anti-GFP results in significant amplification of signal when fluorochrome conjugated polyclonal anti-GFP is used relative to the fluorescence of GFP alone. For immunoblotting use either alkaline phosphatase or peroxidase conjugated anti-GFP to detect GFP or GFP containing proteins on western blots. Optimal titers for applications should be determined by the researcher.

    Western Blot Dilution: 1:3,000 - 1:30,000

    ELISA Dilution: 1:10,000 - 1:30,000

    IF Microscopy Dilution: User Optimized

    Other: User Optimized

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.0 mg/mL

    Buffer

    Buffer: 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2

    Stabilizer: None

    Preservative: 0.01 % (w/v) Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    Store mouse anti-GFP 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. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.

    Date de péremption

    12 months
  • Žaja, Aydin, Lippok, Feederle, Lüscher, Feijs: "Comparative analysis of MACROD1, MACROD2 and TARG1 expression, localisation and interactome." dans: Scientific reports, Vol. 10, Issue 1, pp. 8286, (2020) (PubMed).

    Santos, Damásio, Kun-Rodrigues, Barbot, Sequeiros, Brás, Alonso, Guerreiro: "Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype." dans: Journal of clinical medicine, Vol. 9, Issue 4, (2020) (PubMed).

    Dohmen, Krieg, Agalaridis, Zhu, Shehata, Pfeiffenberger, Amelang, Bütepage, Buerova, Pfaff, Chanda, Geley, Preisinger, Sakamoto, Lüscher, Neumann, Vervoorts: "AMPK-dependent activation of the Cyclin Y/CDK16 complex controls autophagy." dans: Nature communications, Vol. 11, Issue 1, pp. 1032, (2020) (PubMed).

    Santos, Morais, Pereira, Sequeiros, Alonso: "Parkin truncating variants result in a loss-of-function phenotype." dans: Scientific reports, Vol. 9, Issue 1, pp. 16150, (2019) (PubMed).

    Khlghatyan, Evstratova, Chamberland, Marakhovskaia, Bahremand, Toth, Beaulieu: "Mental Illnesses-Associated Fxr1 and Its Negative Regulator Gsk3β Are Modulators of Anxiety and Glutamatergic Neurotransmission." dans: Frontiers in molecular neuroscience, Vol. 11, pp. 119, (2018) (PubMed).

    Terrell, Wu, Tsao, Barber, Servinsky, Payne, Bentley: "Nano-guided cell networks as conveyors of molecular communication." dans: Nature communications, Vol. 6, pp. 8500, (2016) (PubMed).

    Moerdyk-Schauwecker, Shah, Murphy, Hastie, Mukherjee, Grdzelishvili: "Resistance of pancreatic cancer cells to oncolytic vesicular stomatitis virus: role of type I interferon signaling." dans: Virology, Vol. 436, Issue 1, pp. 221-34, (2013) (PubMed).

    Feijs, Kleine, Braczynski, Forst, Herzog, Verheugd, Linzen, Kremmer, Lüscher: "ARTD10 substrate identification on protein microarrays: regulation of GSK3β by mono-ADP-ribosylation." dans: Cell communication and signaling : CCS, Vol. 11, Issue 1, pp. 5, (2013) (PubMed).

    Hastie, Besmer, Shah, Murphy, Moerdyk-Schauwecker, Molestina, Roy, Curry, Mukherjee, Grdzelishvili: "Oncolytic vesicular stomatitis virus in an immunocompetent model of MUC1-positive or MUC1-null pancreatic ductal adenocarcinoma." dans: Journal of virology, Vol. 87, Issue 18, pp. 10283-94, (2013) (PubMed).

    Forst, Karlberg, Herzog, Thorsell, Gross, Feijs, Verheugd, Kursula, Nijmeijer, Kremmer, Kleine, Ladurner, Schüler, Lüscher: "Recognition of mono-ADP-ribosylated ARTD10 substrates by ARTD8 macrodomains." dans: Structure (London, England : 1993), Vol. 21, Issue 3, pp. 462-75, (2013) (PubMed).

    Goel, Sienkiewicz, Picciani, Wang, Lee, Bhattacharya: "Cochlin, intraocular pressure regulation and mechanosensing." dans: PLoS ONE, Vol. 7, Issue 4, pp. e34309, (2012) (PubMed).

    Goel, Sienkiewicz, Picciani, Lee, Bhattacharya: "Cochlin induced TREK-1 co-expression and annexin A2 secretion: role in trabecular meshwork cell elongation and motility." dans: PLoS ONE, Vol. 6, Issue 8, pp. e23070, (2011) (PubMed).

    Jesse, Koenig, Ellenrieder, Menke: "Lef-1 isoforms regulate different target genes and reduce cellular adhesion." dans: International journal of cancer, Vol. 126, Issue 5, pp. 1109-20, (2010) (PubMed).

    Shen, Da Silva, He, Cline: "Type A GABA-receptor-dependent synaptic transmission sculpts dendritic arbor structure in Xenopus tadpoles in vivo." dans: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 29, Issue 15, pp. 5032-43, (2009) (PubMed).

    Forrest, Paden, Allen, Collins, Speck: "ORF73-null murine gammaherpesvirus 68 reveals roles for mLANA and p53 in virus replication." dans: Journal of virology, Vol. 81, Issue 21, pp. 11957-71, (2007) (PubMed).

    Yang, Camp, Gritsenko, Luo, Kelly, Clauss, Brinkley, Smith, Stenoien: "Identification of a novel mitotic phosphorylation motif associated with protein localization to the mitotic apparatus." dans: Journal of cell science, Vol. 120, Issue Pt 22, pp. 4060-70, (2007) (PubMed).

    Koenig, Mueller, Hasel, Adler, Menke: "Collagen type I induces disruption of E-cadherin-mediated cell-cell contacts and promotes proliferation of pancreatic carcinoma cells." dans: Cancer research, Vol. 66, Issue 9, pp. 4662-71, (2006) (PubMed).

  • Antigène

    GFP (Green Fluorescent Protein (GFP))

    Autre désignation

    GFP

    Sujet

    Background: Green fluorescent protein 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.

    UniProt

    P42212
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