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 CHO-K1/Ga15/AMY3 Stable Cell Line

Figure 1. Amylin-induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/Gα15/AMY3 cells. The cells were loaded with Calcium-4 prior to stimulation with an AMY3 receptor agonist, Amylin. The intracellular calcium change was measured by FLIPR. The fluorescence signal were normalized and plotted against the log of the cumulative doses (5-fold dilution) of Amylin (Mean ± SD, n = 4). The EC50 of Amylin on this cells was 0.1747 μM.
Notes:
1. EC50 value is calculated with four parameter logistic equation:
Y=Bottom + (Top-Bottom)/(1+10^((LogEC50-X)*HillSlope))
X is the logarithm of concentration. Y is the response
Y is RFU and starts at Bottom and goes to Top with a sigmoid shape.
2. Signal to background Ratio (S/B) = Top/Bottom

CHO-K1/Ga15/AMY3 Stable Cell Line

Receptor activity-modifying proteins (RAMPs) are a class of protein which interact with and modulate the activities of several Class B G Protein-Coupled Receptors including the receptors for secretin, calcitonin (CT), glucagon, and vasoactive intestinal peptide (VIP).There are three distinct types of RAMPs, designated RAMP1, RAMP2, and RAMP3, each encoded by a separate gene. Currently the function of RAMPs is divided into 2 class activities. Association of RAMPs with either the CT or CALCRL proteins forms 6 different receptors from the calcitonin receptor family. When associated with the Calcitonin receptor (CTR) or Calcitonin receptor-like (CALCRL) RAMPs can change the selectivity of the receptor for a specific hormone. In the cases of the other receptors mentioned however, there is no evidence that they can do this, but instead function to regulate trafficking of receptors from the ER / golgi to the membrane. GenScript's cloned human AMY3–expressing cell line is generated in the CHO-K1/Gα15 host.
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Description

Receptor activity-modifying proteins (RAMPs) are a class of protein which interact with and modulate the activities of several Class B G Protein-Coupled Receptors including the receptors for secretin, calcitonin (CT), glucagon, and vasoactive intestinal peptide (VIP).There are three distinct types of RAMPs, designated RAMP1, RAMP2, and RAMP3, each encoded by a separate gene. Currently the function of RAMPs is divided into 2 class activities. Association of RAMPs with either the CT or CALCRL proteins forms 6 different receptors from the calcitonin receptor family. When associated with the Calcitonin receptor (CTR) or Calcitonin receptor-like (CALCRL) RAMPs can change the selectivity of the receptor for a specific hormone. In the cases of the other receptors mentioned however, there is no evidence that they can do this, but instead function to regulate trafficking of receptors from the ER / golgi to the membrane. GenScript's cloned human AMY3–expressing cell line is generated in the CHO-K1/Gα15 host.

Synonyms

RAMP3+CALCR

Applications Functional assay for AMY3 receptor

Storage Liquid nitrogen immediately upon delivery

Freeze Medium 45% culture medium, 45% FBS (Cat. #10099-141, Gibco), 10% DMSO (Cat. #D2650, Sigma)
Culture Medium Ham’s F-12K (Kaighn’s), 10% FBS, 200 μg/ml Zeocin (Cat. #R250-01, Life Technologies), 400 μg/ml G418 (Cat. #10131-035, Gibco), 100 μg/ml Hygromycin B (Cat. #10687010, Invitrogen)

  •  CHO-K1/Ga15/AMY3 Stable Cell Line
  •  CHO-K1/Ga15/AMY3 Stable Cell Line

    Figure 1. Amylin-induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/Gα15/AMY3 cells. The cells were loaded with Calcium-4 prior to stimulation with an AMY3 receptor agonist, Amylin. The intracellular calcium change was measured by FLIPR. The fluorescence signal were normalized and plotted against the log of the cumulative doses (5-fold dilution) of Amylin (Mean ± SD, n = 4). The EC50 of Amylin on this cells was 0.1747 μM.
    Notes:
    1. EC50 value is calculated with four parameter logistic equation:
    Y=Bottom + (Top-Bottom)/(1+10^((LogEC50-X)*HillSlope))
    X is the logarithm of concentration. Y is the response
    Y is RFU and starts at Bottom and goes to Top with a sigmoid shape.
    2. Signal to background Ratio (S/B) = Top/Bottom


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