Multiplex Assay Kit for Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay)

RIC4; SEC9; SNAP; SUP; Super protein; Resistance To Inhibitors Of Cholinesterase 4 Homolog

(Note: Up to 8-plex in one testing reaction)

  • Product No.LMC955Mi
  • Organism SpeciesHomo sapiens (Human), Mus musculus (Mouse), Rattus norvegicus (Rat), Oryctolagus cuniculus (Rabbit), Sus scrofa; Porcine (Pig), Bos taurus; Bovine (Cattle), Equus caballus; Equine (Horse), Chicken (Gallus) Same name, Different species.
  • Sample TypeTissue homogenates, cell lysates and other biological fluids
  • Test MethodDouble-antibody Sandwich
  • Assay Length3.5h
  • Detection Range0.01-10ng/mL
  • SensitivityThe minimum detectable dose of this kit is typically less than 0.003 ng/mL.
  • DownloadInstruction Manual
  • UOM 8Plex 7Plex 6Plex 5Plex 4Plex 3Plex 2Plex1Plex
  • FOB US$ 437  US$ 454  US$ 479  US$ 512  US$ 546  US$ 596  US$ 672  US$ 840  Add to Price Calculator Result
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Specificity

This assay has high sensitivity for detection of Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay).
100% cross-reactivity of Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay) was observed among Human, Mouse, Rat, Rabbit, Porcine, Bovine, Equine, Gallus.

Recovery

Matrices listed below were spiked with certain level of recombinant Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay) and the recovery rates were calculated by comparing the measured value to the expected amount of Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 92-101 97
EDTA plasma(n=5) 86-95 91
heparin plasma(n=5) 90-104 97
sodium citrate plasma(n=5) 87-101 93

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Synaptosomal Associated Protein 25kDa (SNAP25) ,etc. by FLIA (Flow Luminescence Immunoassay) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample 1:2 1:4 1:8 1:16
serum(n=5) 84-101% 95-104% 89-101% 84-92%
EDTA plasma(n=5) 90-99% 97-104% 93-101% 99-105%
heparin plasma(n=5) 87-94% 78-103% 98-105% 80-97%
sodium citrate plasma(n=5) 86-97% 89-104% 84-94% 88-103%

Stability

The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Reagents and materials provided

Reagents Quantity Reagents Quantity
96-well plate 1 Plate sealer for 96 wells 4
Pre-Mixed Standard 2 Standard Diluent 1×20mL
Pre-Mixed Magnetic beads (22#:SNAP25) 1 Analysis buffer 1×20mL
Pre-Mixed Detection Reagent A 1×120μL Assay Diluent A 1×12mL
Detection Reagent B (PE-SA) 1×120μL Assay Diluent B 1×12mL
Sheath Fluid 1×10mL Wash Buffer (30 × concentrate) 1×20mL
Instruction manual 1

Assay procedure summary

1. Preparation of standards, reagents and samples before the experiment;
2. Add 100μL standard or sample to each well,
    add 10μL magnetic beads, and incubate 90min at 37°C on shaker;
3. Remove liquid on magnetic frame, add 100μL prepared Detection Reagent A. Incubate 60min at 37°C on shaker;
4. Wash plate on magnetic frame for three times;
5. Add 100μL prepared Detection Reagent B, and incubate 30 min at 37°C on shaker;
6. Wash plate on magnetic frame for three times;
7. Add 100μL sheath solution, swirl for 2 minutes, read on the machine.

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