Human Lysophosphatidic Acid Receptor 1 (LPAR1) ELISA Kit
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Human Lysophosphatidic Acid Receptor 1 (LPAR1) ELISA Kit

Cat.No: HTK-HMM-0001 Datasheet

Specification Quantities

48T:
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96T:
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96T*5:
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96T*10:
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96T*100:
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Product Details Related Products
Product Name Human Lysophosphatidic Acid Receptor 1 (LPAR1) ELISA Kit
Catalog No. HTK-HMM-0001
Description LPAR1 (lysophosphatidic acid receptor 1) is an important G protein-coupled receptor in the human body, which plays an important role in physiological processes such as cell signaling, cell proliferation, cell migration, and cell adhesion. During these physiological processes, LPAR1 can bind to lysosomal acid-like deoxygenated neuronal activation precursor (LPA) produced by lysosomes and mediate cellular signaling. Activation of LPAR1 leads to an increase in intracellular calcium concentration, which in turn activates a variety of signaling pathways and affects cellular function.
Test Species Human
Synonyms EDG2; Gpcr26; LPA1; Mrec1.3; edg-2; rec.1.3; vzg-1; Endothelial Differentiation, Lysophosphatidic Acid G-Protein-Coupled Receptor 2
Applications This kit is used for the detection of Lysophosphatidic Acid Receptor 1 (LPAR1), which is detected without significant cross-reactivity with other similar substances.
Sample Type Tissue homogenates, cell lysates and other biological fluids.
Detection Methods Sandwich ELISA
Estimated Measurement Time 3 h
Detection Range 0.312-20 ng/mL
Sensitivity 0.112 ng/mL
Accuracy Intra-lot variation: CV<10%; Inter-lot variation: CV<12%.
Detection Principle The lysophosphatidic acid receptor 1(LPAR1) antibody is coated in a 96-well microplate to form a solid-phase carrier. Standards or specimens are added to the microplates, respectively, and the lysophosphatidic acid receptor 1(LPAR1) is bound to the antibody attached to the solid-phase carrier. Then, the biotinylated lysophosphatidic acid receptor 1(LPAR1) antibody is added. After washing off the unbound biotinylated antibodies, add HRP-labeled avidin, thoroughly wash again, and then add TMB substrate for color development. TMB is converted into blue under the catalysis of peroxidase and then into the final yellow under the action of acid. The depth of color is positively correlated with lysophosphatidic acid receptor 1(LPAR1) in the sample. The absorbance (O.D. value) is measured at a wavelength of 450nm using a microplate reader, and the sample concentration is calculated.
Procedures 1. Preparation of standards, reagents, and samples before the experiment; 2. Add 100 µL of sample (standard and sample) and incubate at 37°C for 1 hour; 3. Aspirate, add Detection Solution A 100 µL, incubate at 37°C for 1 hour; 4. Wash the plate 3 times; 5. Add 100 µL of Detection Solution B and incubate at 37°C for 30 minutes. 6. Wash the plate 5 times; 7. Add TMB Substrate 90 µL, incubate at 37°C for 10-20 minutes. 8. Add 50 µL of Termination Solution and read at 450 nm immediately.
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