Revision 7

#4339Store at -20C

Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
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Product Information

Storage

Please keep all kit components in -20°C before use.

Specificity / Sensitivity

The immunoreactivity of this kit was tested against the following: ADP, AMP, ATP, cAMP, cGMP, cIMP, cTMP, CTP, GDP, GMP and GTP. Relatively minor cross-reactivity was observed with cGMP and cIMP, with 10 fold higher sensitivity for cAMP compared to either cGMP or cIMP. No cross-reactivity was observed with any of the other factors tested. Kit sensitivity, as shown in Figure 1, demonstrates a dynamic range of 0.2 to 12 nM of cAMP. Changes in cellular cAMP levels following specific treatments are shown in Figure 2 (CHO cells) and Figure 3 (293 cells).

Species Reactivity:

All Species Expected

Product Description

The Cyclic AMP XP® Assay Kit is a competition enzyme-linked immunoassay used to determine cAMP levels in cells or tissues of interest. In this assay, cAMP found in test sample competes with a fixed amount of HRP-linked cAMP for binding to an anti-cAMP XP® Rabbit mAb immobilized onto a 96-well plate. Following washing to remove excess sample cAMP and HRP-linked cAMP, HRP substrate TMB is added to develop color. Because of the competitive nature of this assay, the magnitude of the absorbance for this developed color is inversely proportional to the quantity of sample cAMP. Measurement of absorbance using the cAMP Standard allows calculating the absolute amount of cAMP in a sample of interest.
Note: 12, 8-well modules -Each module is designed to break apart for 8 tests.

Background

Cyclic adenosine 3’,5’-monophosphate (cAMP) is an important second messenger involved in many signal transduction pathways in different cell types of numerous species (1-3). In mammalian cells this important molecule is produced by adenylyl cyclases (AC). Extracellular stimuli such as neurotransmitters, hormones, chemokines, lipid mediators and drugs, can modulate AC activity to increase or decrease cAMP production by binding to a large number of transmembrane G protein-coupled receptors (4). The degradation of cAMP to AMP is catalyzed by phosphodiesterases that are regulated by intracellular nucleotide concentrations, phosphorylation, or binding of Ca2+/calmodulin and other regulatory proteins (5). A set of diverse molecules, including cAMP-dependent protein kinase (PKA), cyclic nucleotide-gated ion channels, and exchange proteins that are activated by cAMP (Epac), mediate downstream cAMP signaling (6,7). cAMP modulates various biological processes including metabolism, differentiation, cardiac cell functions, neuronal signaling, cell adhesion, and immune functions (5-7).

  1. Serezani, C.H. et al. (2008) Am J Respir Cell Mol Biol 39, 127-32.
  2. Beavo, J.A. and Brunton, L.L. (2002) Nat Rev Mol Cell Biol 3, 710-8.
  3. Kopperud, R. et al. (2003) FEBS Lett 546, 121-6.
  4. Kamenetsky, M. et al. (2006) J Mol Biol 362, 623-39.
  5. Cheng, J. and Grande, J.P. (2007) Exp Biol Med (Maywood) 232, 38-51.
  6. Holz, G.G. et al. (2006) J Physiol 577, 5-15.
  7. Taylor, S.S. et al. (2008) Biochim Biophys Acta 1784, 16-26.

Species Reactivity

Species reactivity is determined by testing in at least one approved application (e.g., western blot).

Cross-Reactivity Key

H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

Trademarks and Patents

Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
XP is a registered trademark of Cell Signaling Technology, Inc.
All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

限制使用

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Revision 7
#4339

Cyclic AMP XP® Assay Kit

Cyclic AMP XP® Assay Kit: Image 1 Expand Image
图 1:cAMP 标准液用 1X Cell Lysis Buffer #9803 稀释,并且样品遵照 Cyclic AMP XP® Assay Kit 实验步骤进行检测。该标准曲线仅用作演示目的;用户应为每个样品组制成标准曲线,以准确确定 cAMP 浓度。
Cyclic AMP XP® Assay Kit: Image 2 Expand Image
图 2:使用 Cyclic AMP XP® Assay Kit #4339 检测发现,CHO 细胞用 Forskolin #3828 处理会增加 cAMP 浓度。CHO 细胞按 4x104 个细胞/孔放在 96 孔板上进行培养,并孵育过夜。细胞未经处理或用 0.5 mM IBMX 预处理 30 分钟,随后进行 forskolin 处理(15 分钟)并用 1X Cell Lysis Buffer #9803 进行裂解。吸光度值(左图)和活性百分比(右图)如上所示。活性百分比计算如下:% 活性 = 100x [(A-A本底)/(A最大-A本底)],其中 A 为样品吸光度,A最大为最大刺激(即高 forskolin 浓度)时的吸光度,A 本底为在本底水平(无 forskolin)时的吸光度。Forskolin 会直接激活腺苷酸环化酶,并使细胞 cAMP 浓度升高。IBMX 是 cAMP 和 cGMP 磷酸二酯酶的一种非特异性抑制剂,能促进 cAMP 和 cGMP 在细胞中聚集。
Cyclic AMP XP® Assay Kit: Image 3 Expand Image
图 3:293 细胞用异丙肾上腺素处理会导致 cAMP 浓度升高,使用 Cyclic AMP XP® Assay Kit #4339 可进行检测。293 细胞按 3x104 个细胞/孔在 96 孔板中培养,并孵育过夜。细胞用 0.5 mM IBMX 预处理 30 分钟,随后进行异丙肾上腺素处理(3 分钟)并用 1X Cell Lysis Buffer #9803 进行裂解。吸光度值(左图)和活性百分比(右图)如上所示。活动百分比计算如下:% 活性 = 100* [(A-A本底)/(A最大-A本底)],其中 A 为样品吸光度,A最大为最大刺激(即高异丙肾上腺素浓度)时的吸光度,A 本底为在本底水平(无异丙肾上腺素)时的吸光度。异丙肾上腺素是一种 β-肾上腺受体激动剂,并能激活在 293 细胞中呈内源性表达的 β-2 肾上腺素能受体 (ADRB2)。ADRB2 激活会导致腺苷酸环化酶激活以及 cAMP 合成为其第二信使。