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- 详细信息
- 文献和实验
- 技术资料
- 库存:
50
- 供应商:
LSM BIO
- 检测范围:
78-5000pg/ml
- 检测方法:
夹心法ELISA或竞争法ELISA
- 应用:
检测小鼠血清,血浆,组织匀浆内的目标蛋白含量
- 适应物种:
小鼠
- 标记物:
Small G protein signaling modulator 1, Sgsm1
- 样本:
小鼠血清,血浆,组织匀浆
- 灵敏度:
39pg/ml
- 规格:
96Tests
Mouse Small G protein signaling modulator 1, Sgsm1 ELISA KIT
Product Name:Mouse Small G protein signaling modulator 1, Sgsm1 ELISA KIT
Packing:96T
Catalog No.:ELI-13515m
Gene Name:Mouse Sgsm1
Detect Range:0.156-10ng/ml
Sensitivity:0.094ng/ml
Target Protein Name:Mouse Sgsm1
Alternative Name:Mouse Small G protein signaling modulator 1, Sgsm1
Sample type:serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA type:Sandwich ELISA Kit
Product Description:Mouse Small G protein signaling modulator 1, Sgsm1 ELISA KIT allows for the in vitro quantitative determination of Mouse Sgsm1 concentrations in serum, plasma, tissue homogenates, cell culture supernates or other biological fluids.
ELISA Test Principle:
The microtiter plate provided in Mouse Small G protein signaling modulator 1, Sgsm1 ELISA KIT has been pre-coated with an Mouse Small G protein signaling modulator 1, Sgsm1 antibody specific to Mouse Sgsm1 .Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for Mouse Sgsm1 and then avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. Only those wells that contain Mouse Sgsm1 , biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm.The concentration of Mouse Sgsm1 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
NOTE:FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS! PLEASE READ ENTIRE PROCEDURE!
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文献和实验The CRE Luc Mouse Model for Bioimaging Ligand Activation of G Protein-Coupled Receptors
from a luciferase reporter have been used extensively in vitro with high-throughput screens (HTS) of large chemical compound libraries. We have generated a transgenic mouse model (CRE luc) with a luciferase reporter under the control of a synthetic promoter
Overview of Formation of G‐Quadruplex Structures
. Kan, Z.Y., Lin, Y., Wang, F., Zhuang, X.Y., Zhao, Y., Pang, D.W., Hao, Y.H., and Tan, Z. 2007. G‐quadruplex formation in human telomeric (TTAGGG)4 sequence with complementary strand in close vicinity
Study of MAPK Signaling Using Knockout Mice
The p42 and p44 mitogen-activated protein kinases (MAPKs) (p42/p44 MAPK, Erk2 /Erk1) are activated through the small G protein Ras and sequential activation of the protein kinases Raf and MEK on stimulation of cells with a broad range
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