Human Lysophosphatidylglycerol Acyltransferase 1 (LPGAT1) Multiplex Assay Kit-FLIA
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Human Lysophosphatidylglycerol Acyltransferase 1 (LPGAT1) Multiplex Assay Kit-FLIA

Cat.No: HTK-HMM-0008 Datasheet

Specification Quantities

8 Indicators:
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7 Indicators:
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6 Indicators:
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5 Indicators:
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4 Indicators:
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3 Indicators:
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2 Indicators:
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1 Indicator:
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Product Details Related Products
Product Name Human Lysophosphatidylglycerol Acyltransferase 1 (LPGAT1) Multiplex Assay Kit-FLIA
Catalog No. HTK-HMM-0008
Description LPGAT1 encodes a protein belonging to the lysophospholipid acyltransferase family, whose function involves cell membrane remodeling and cardiolipin synthesis, which is essential for maintaining cell membrane stability and function.
Test Species Human
Synonyms FAM34A1; NET8; Family With Sequence Similarity 34, Member A
Applications This kit is used for the detection of lysophosphatidylglycerol acyltransferase 1 (LPGAT1) and other multi-factors, and there is no significant cross-reactivity with other similar substances after testing. No more than 8 indicators of multi-factors can be mixed in a single test.
Sample Type Tissue homogenates, cell lysates and other biological fluids.
Detection Methods FLIA
Estimated Measurement Time 3.5 h
Detection Range 0.01-10 ng/mL
Sensitivity 0.003 ng/mL
Accuracy Intra-lot variation: CV<10%; Inter-lot variation: CV<12%.
Detection Principle The antibodies of the multi-factor detection kit (flow fluorescence luminescence method), such as lysolytic phosphatidylglycerol acyltransferase 1(LPGAT1), are coated on magnetic beads to prepare solid-phase carriers. Standards or specimens and magnetic beads are added to the microwells, respectively. Among them, the multi-factor detection kits, such as lysophosphatidylglycerol acyltransferase 1(LPGAT1) (flow cytometry fluorescence luminescence method) are combined with the antibodies linked to the solid-phase carrier, and then biotinylated antibodies such as lysophosphatidylglycerol acyltransferase 1(LPGAT1) and other multi-factor detection kits (flow cytometry fluorescence luminescence method) are added. After washing off the unbound biotinylated antibodies, add PE-labeled avidin, and thoroughly wash again before taking the readings on the machine. The MFI value is positively correlated with the multi-factor detection kits such as lysophosphatidylglycerol acyltransferase 1(LPGAT1) in the samples (flow cytometry fluorescence spectrometry).
Procedures 1. Prepare standards, reagents, and samples before the experiment; 2. Add samples (standards, samples, magnetic beads) 100 μL of standards or samples and 10 μL of magnetic beads, and incubate for 90 minutes at 37°C on an enzyme plate oscillator; 3. Drain the plate magnetically, add 100 μL of Detection Solution A, and incubate at 37°C for 60 minutes; 4. Wash the plate 3 times with magnetic suction; 5. Add 100 μL of Detection Solution B and incubate at 37°C for 30 minutes with shaking; 6. Wash the plate 3 times with magnetic suction; 7. Add 100μL of Sheath Solution, vortex for 2 minutes, and read.
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