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Cathelicidin Kit ELISA

CAMP Reactivité: Chemical Colorimetric Competition ELISA Plasma, Urine
N° du produit ABIN2345105
  • Antigène Voir toutes Cathelicidin (CAMP) Kits ELISA
    Cathelicidin (CAMP) (Cathelicidin Antimicrobial Peptide (CAMP))
    Reactivité
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Chemical
    Méthode de détection
    Colorimetric
    Type de méthode
    Competition ELISA
    Application
    ELISA
    Type d'échantillon
    Plasma, Urine
    Analytical Method
    Quantitative
    Sensibilité
    1 pmol/mL
    Attributs du produit
    cAMP ELISA Kit is a competitive enzyme immunoassay designed to measure cAMP in cell culture supernatants, plasma, serum, saliva, urine, and cell lysates. The kit selectively measures cAMP levels without any significant cross reactivities to other nucleotides or cyclic nucleotides. Samples containing low cAMP levels may be acetylated (reagents provided) for increased sensitivity. Under non-acetylated conditions, the kit has a detection range of 1 to 1000 pmol/mL cAMP, however, under acetylated conditions, the sensitivity is enhanced (approx 100X) to a detection range of 10-2500 fmol/mL.
    Ingrédients
    1. Goat Anti-Rabbit Antibody Coated Plate : One strip well 96-well plate.
    2. cAMP Standard : One 100 μL vial provided at 10 mM.
    3. Rabbit Anti-cAMP Polyclonal Antibody : One 15 μL vial.
    4. Peroxidase cAMP Tracer Conjugate : One 30 μL vial.
    5. Assay Diluent : One 25 mL bottle.
    6. Lysis Buffer : One 50 mL bottle.
    7. 10X Wash Buffer : One 50 mL bottle.
    8. Triethylamine : One 2 mL amber bottle.
    9. Acetic Anhydride : One 1 mL amber bottle.
    10. Substrate Solution : One 12 mL amber bottle.
    11. Stop Solution (Part. No. 310808): One 12 mL bottle.
    Matériel non inclus
    1. Orbital plate shaker
    2. 10 μL to 1000 μL adjustable single channel micropipettes with disposable tips
    3. 50 μL to 300 μL adjustable multichannel micropipette with disposable tips
    4. Multichannel micropipette reservoir
    5. Microplate reader capable of reading at 450 nm (620 nm as optional reference wave length)
    6. Glass or polypropylene tubes for acetylated samples and standards
    Top Product
    Discover our top product CAMP Kit ELISA
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Commentaires

    • Sensitivity as low as 1 pmol/mL
    • Suitable for use with cell and tissue lysates, urine, plasma, or culture medium
    • Convenient strip-well plate format

    Plaque
    Uncoated
    Protocole
    An anti-Rabbit IgG polyclonal coating antibody is adsorbed onto a microtiter plate. Cyclic AMP present in the sample or standard competes with Peroxidase cAMP Tracer for plate binding, in the presence of Rabbit Anti-cAMP Polyclonal Antibody. Following incubation and wash steps, any Peroxidase cAMP Tracer bound to the plate is detected with addition of Substrate Solution. The colored product formed in inversely proportional to the amount of cAMP present in the sample. The reaction is terminated by addition of acid and absorbance is measured at 450 nm. A standard curve is prepared from cAMP Standard and sample concentration is then determined.
    Préparation des réactifs
    • 1X Wash Buffer: Dilute the 10X Wash Buffer Concentrate to 1X with deionized water. Stir to homogeneity.
    • Rabbit Anti-cAMP Polyclonal Antibody: Immediately before use dilute the Rabbit Anti-cAMP Antibody 1:500 with Assay Diluent. Do not store diluted solutions. 3
    • Peroxidase cAMP Tracer Conjugate: Immediately before use dilute the Peroxidase cAMP Tracer Conjugate 1:100 with Assay Diluent. Do not store diluted solutions.
    • Acetylation Reagent: Preparation of the Acetylation Reagent should be done in glass tubes and in a fume hood. The Acetylation Reagent is made by mixing Acetic Anhydride with Triethylamine at a 1:2 ratio (example: 0.5 mL Acetic Anhydride + 1 mL Triethylamine). Use the reagent within 60 minutes of preparation. Caution: The components of this reagent are known to be caustic, corrosive, flammable, and lachrymators. Use appropriate protection when handling. Preparation of cAMP Standards (Non-Acetylated Version) 1. Thaw the cAMP Standard at room temperature and mix thoroughly by pipetting (cAMP can precipitate when frozen but will redissolve when mixed well). Freshly prepare a dilution series of cAMP Standard in the concentration range of 100 μM - 100 pM by diluting the cAMP Standard in Lysis Buffer (Table 1). Lysis Buffer cAMP Standard Tubes cAMP Standard (μL) (μL) Concentration 1 10 990 100 μM 2 20 of Tube #1 180 10 μM 3 20 of Tube #2 180 1 μM 4 20 of Tube #3 180 100 nM 5 20 of Tube #4 180 10 nM 6 20 of Tube #5 180 1 nM 7 20 of Tube #6 180 100 pM 8 0 180 0 Table 1.
    Procédure de l'essai
    1. Prepare and mix all reagents thoroughly before use.
    2. Each cAMP sample, cAMP Standard, and blank should be assayed in duplicate. Note: cAMP samples must be compared with corresponding standards (i.e. acetylated samples compared with acetylated standards, non-acetylated samples with non-acetylated standards).
    3. Add 50 μL of cAMP sample or standard (acetylated or non-acetylated) to the Goat Anti-Rabbit Antibody Coated Plate.
    4. Add 25 μL of diluted Peroxidase cAMP Tracer Conjugate (see Preparation of Reagents Section) to each tested well.
    5. Add 50 μL of diluted Rabbit Anti-cAMP Polyclonal Antibody (see Preparation of Reagents Section) to each tested well.
    6. Cover with a Plate Cover and incubate at room temperature for 2 hours with shaking.
    7. Remove Plate Cover and empty wells. Wash microwell strips 5 times with 250 μL 1X Wash Buffer per well with thorough aspiration between each wash. After the last wash, empty wells and tap microwell strips on absorbent pad or paper towel to remove excess 1X Wash Buffer.
    8. Warm Substrate Solution to room temperature. Add 100 μL of Substrate Solution to each well, including the blank wells. Incubate at room temperature for 5-20 minutes on an orbital shaker.
    9. Stop the enzyme reaction by adding 100 μL of Stop Solution into each well, including the blank wells. Results should be read immediately (color will fade over time).
    10. Read absorbance of each microwell on a spectrophotometer using 450 nm as the primary wave length. 6
    Restrictions
    For Research Use only
  • Stock
    4 °C/-20 °C
    Stockage commentaire
    Store kit components at 4°C. For longer term use, store the Rabbit Anti-cAMP Polyclonal Antibody at -20°C.
  • Meng, Liang, Chen, Luo, Bai, Li, Zhang, Xiao, He, Zhang, Xu, Xiao, Liu, Hu, Liu: "Rheb Inhibits Beigeing of White Adipose Tissue via PDE4D5-dependent Down-regulation of the cAMP-PKA Signaling Pathway." dans: Diabetes, (2017) (PubMed).

    Zhao, Ho, Wang, Bi, Yemul, Ward, Freire, Mazzola, Brathwaite, Mezei, Sanchez, Elder, Pasinetti: "In Silico Modelling of Novel Drug Ligands Associated with Abnormal Tau Phosphorylation: Implications for Concussion Associated Tauopathy Intervention." dans: Journal of cellular biochemistry, (2016) (PubMed).

    Iyer, Ranjan, Elias, Parrales, Sasaki, Roy, Umar, Tawfik, Iwakuma: "Genome-wide RNAi screening identifies TMIGD3 isoform1 as a suppressor of NF-κB and osteosarcoma progression." dans: Nature communications, Vol. 7, pp. 13561, (2016) (PubMed).

    Trehan, Rotgers, Coffey, Huhtaniemi, Rivero-Müller: "CANDLES, an assay for monitoring GPCR induced cAMP generation in cell cultures." dans: Cell communication and signaling : CCS, Vol. 12, pp. 70, (2015) (PubMed).

    Cortés, Amigo, Zanlungo, Galgani, Robledo, Arrese, Bozinovic, Nervi: "Metabolic effects of cholecystectomy: gallbladder ablation increases basal metabolic rate through G-protein coupled bile acid receptor Gpbar1-dependent mechanisms in mice." dans: PLoS ONE, Vol. 10, Issue 3, pp. e0118478, (2015) (PubMed).

    Liu, Ma, Li, Huang, Li, Tao, Ma: "?-Arrestin-biased signaling mediates memory reconsolidation." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 112, Issue 14, pp. 4483-8, (2015) (PubMed).

    Rose, Yu, Heinzer, Harrast, Fan, Raike, Thompson, Pare, Weinshenker, Smith, Jinnah, Hess: "A new knock-in mouse model of l-DOPA-responsive dystonia." dans: Brain : a journal of neurology, Vol. 138, Issue Pt 10, pp. 2987-3002, (2015) (PubMed).

    Omosun, McKeithen, Ryans, Kibakaya, Blas-Machado, Li, Singh, Inoue, Xiong, Eko, Black, Igietseme, He: "Interleukin-10 modulates antigen presentation by dendritic cells through regulation of NLRP3 inflammasome assembly during Chlamydia infection." dans: Infection and immunity, Vol. 83, Issue 12, pp. 4662-72, (2015) (PubMed).

    He, Santhanam, Lu, dUscio, Katusic: "Role of prostacyclin signaling in endothelial production of soluble amyloid precursor protein-? in cerebral microvessels." dans: Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, (2015) (PubMed).

    Jones, Kainz, Khan, Lee, Carrithers: "Human macrophage SCN5A activates an innate immune signaling pathway for antiviral host defense." dans: The Journal of biological chemistry, Vol. 289, Issue 51, pp. 35326-40, (2014) (PubMed).

    Chen, Bai, Tian, Du, Chen: "Identification of serine 348 on the apelin receptor as a novel regulatory phosphorylation site in apelin-13-induced G protein-independent biased signaling." dans: The Journal of biological chemistry, Vol. 289, Issue 45, pp. 31173-87, (2014) (PubMed).

    Rachmin, Tshori, Smith, Oppenheim, Marchetto, Kay, Foo, Dagan, Golomb, Gilon, Borg, Razin: "Erbin is a negative modulator of cardiac hypertrophy." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 111, Issue 16, pp. 5902-7, (2014) (PubMed).

    Tian, Ni, Guo, Liu, Dang, Guo, Zhang: "TSH stimulates the proliferation of vascular smooth muscle cells." dans: Endocrine, Vol. 46, Issue 3, pp. 651-8, (2014) (PubMed).

    Yong, Ming, Feng, Chun, Hua: "Electromagnetic fields promote osteogenesis of rat mesenchymal stem cells through the PKA and ERK1/2 pathways." dans: Journal of tissue engineering and regenerative medicine, (2014) (PubMed).

    Smith, An, Wagner, Lewis, Cohen, Li, Mahbod, Sandoval, Perez-Tilve, Tamarina, Philipson, Stoffers, Seeley, DAlessio: "The role of ? cell glucagon-like peptide-1 signaling in glucose regulation and response to diabetes drugs." dans: Cell metabolism, Vol. 19, Issue 6, pp. 1050-7, (2014) (PubMed).

    McRobie, King, Fanutti, Symmons, Coussons: "Agouti signalling protein is an inverse agonist to the wildtype and agonist to the melanic variant of the melanocortin-1 receptor in the grey squirrel (Sciurus carolinensis)." dans: FEBS letters, Vol. 588, Issue 14, pp. 2335-43, (2014) (PubMed).

    Peterson, De La Rosa, Eboda, Cilwa, Agarwal, Buchman, Cederna, Xi, Morris, Herndon, Xiao, Tompkins, Krebsbach, Wang, Levi: "Treatment of heterotopic ossification through remote ATP hydrolysis." dans: Science translational medicine, Vol. 6, Issue 255, pp. 255ra132, (2014) (PubMed).

    Terunuma, Haydon, Pangalos, Moss: "Purinergic receptor activation facilitates astrocytic GABAB receptor calcium signalling." dans: Neuropharmacology, Vol. 88, pp. 74-81, (2014) (PubMed).

    Meyer, Giddens, Schaefer, Hall: "GPR37 and GPR37L1 are receptors for the neuroprotective and glioprotective factors prosaptide and prosaposin." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 110, Issue 23, pp. 9529-34, (2013) (PubMed).

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  • Antigène Voir toutes Cathelicidin (CAMP) Kits ELISA
    Cathelicidin (CAMP) (Cathelicidin Antimicrobial Peptide (CAMP))
    Autre désignation
    cAMP (CAMP Produits)
    Synonymes
    CAP-18 Kit ELISA, CAP18 Kit ELISA, CRAMP Kit ELISA, FALL-39 Kit ELISA, FALL39 Kit ELISA, LL37 Kit ELISA, CATH-2 Kit ELISA, Cnlp Kit ELISA, Cramp Kit ELISA, MCLP Kit ELISA, CATH-B1 Kit ELISA, CATHB1 Kit ELISA, CATHL2 Kit ELISA, CATHL7 Kit ELISA, CAP11 Kit ELISA, cathelicidin antimicrobial peptide Kit ELISA, CAMP Kit ELISA, LOC100136187 Kit ELISA, LOC100136439 Kit ELISA, Camp Kit ELISA
    Classe de substances
    Chemical
    Sujet
    Adenosine 3',5'-cyclic monophosphate (cAMP) is a ubiquitous second messenger involved in various cellular activities in many cell and tissue types. It is converted from adenosine triphosphate (ATP) via adenylyl cyclases (AC), and is inactivated by hydrolysis to 5´-AMP by the actions of phosphodiesterases. cAMP may affect cellular function through several different mechanisms including the activation of cAMP-dependent Protein Kinase (PKA), Guanine Nucleotide Exchange Factors (GEFs), and Cyclic Nucleotide-gated (CNG) channels. PKA is a heterotetramer consisting of 2 regulatory (R) subunits and 2 catalytic (C) subunits. Two cAMP molecules bind cooperatively to 2 sites on each R subunit, releasing the active C subunit monomers to phosphorylate a range of downstream substrates. GEFs facilitate the exchange of GDP for GTP and, therefore, promote the activity of G proteins. Exchange Protein Activated by cAMP (Epac) 1 and 2 are GEFs activated upon binding to cAMP. Epac 1 and 2 have been implicated in regulating the activity of the small GTPase Rap-1 (26, 27). CNG channels are cation channels activated by cGMP and/or cAMP. These channels regulate membrane potential, and due to their Ca2+ permeability, can alter the levels of intracellular Ca2+.
    Pathways
    Cellular Response to Molecule of Bacterial Origin
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