Figure 1. α-CGRP induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/Gα15/AMY1 and CHO-K1/Gα15 cells. The cells were loaded with Calcium-4 prior to stimulation with agonist α-CGRP. 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 α-CGRP (Mean ± SD, n = 4). The EC₅₀ of α-CGRP on this cell was 58.8 nM.
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/Gα15/AMY1 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 AMY1–expressing cell line is generated in the CHO-K1/Gα15 host.

产品编号	M00557
规格	2 vials 定制报价
数量
价格	￥85000


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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 AMY1–expressing cell line is generated in the CHO-K1/Gα15 host.

Synonyms

Gene Synonyms: RAMP1+CALCR

产品概述

Applications

Functional assay for AMY1 receptor

产品简介

Storage

Liquid nitrogen immediately upon delivery

培养条件

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), 100 μg/ml Hygromycin B (Cat. #10687010, Invitrogen)

图例

Figure 1. α-CGRP induced concentration-dependent stimulation of intracellular calcium mobilization in CHO-K1/Gα15/AMY1 and CHO-K1/Gα15 cells. The cells were loaded with Calcium-4 prior to stimulation with agonist α-CGRP. 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 α-CGRP (Mean ± SD, n = 4). The EC₅₀ of α-CGRP on this cell was 58.8 nM.
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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CHO-K1/Gα15/AMY1 Stable Cell Line

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