Multiplex Assay Kit for Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1) ,etc. by FLIA (Flow Luminescence Immu
Ref: CC-LMC615Mu
96T
Información del producto
Multiplex Assay Kit for Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1) ,etc. by FLIA (Flow Luminescence Immunoassay)
Información adicional
Stabillity at RT
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
Applications
FLIA Kit for Antigen Detection.
Detection Range
0.01-10ng/mL
Sensitivity
The minimum detectable dose of this kit is typically less than 0.003 ng/mL
Specificity
No significant cross-reactivity or interference between Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1) ,etc. by FLIA (Flow Luminescence Immunoassay) and analogues was observed.
This assay has high sensitivity and excellent specificity for detection of Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1) ,etc. by FLIA (Flow Luminescence Immunoassay).
Research Area
FLIA Kit for Antigen Detection.
Organism species
Mus musculus (Mouse)
Alternative Names
BCL2L3
Bcl-2-like protein 3
Bcl-2-related protein EAT/mcl1
EAT
MCL1L
MCL1S
Myeloid Cell Leukemia Sequence 1, Bcl2 Related
TM
mcl1/EAT
Bcl-2-like protein 3
Bcl-2-related protein EAT/mcl1
EAT
MCL1L
MCL1S
Myeloid Cell Leukemia Sequence 1, Bcl2 Related
TM
mcl1/EAT
Item Name
Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1
Assay Length
3h
Method
Double-antibody Sandwich
Sample Type
Serum, plasma, tissue homogenates and other biological fluids
Format
48T, 96T, 96T×5, 96T×10, 96T×100
Assay Procedure
Double-antibody Sandwich
Test Principle
Analyte-specific antibodies are pre-coated onto color-coded microparticles. Microparticles, standards, and samples are pipetted into wells and the immobilized antibodies bind the analytes of interest. After washing away any unbound substances, a biotinyla
proportional to the concentration of analytes of interest in the sample.
proportional to the concentration of analytes of interest in the sample.
Precision
CV(%) = SD/meanX100
Inter-Assay: CV<12%
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1) ,etc. by FLIA (Flow Luminescence Immunoassay) were tested on 3 different plates, 8 replicates in
Intra-Assay: CV<10%
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Induced Myeloid Leukemia Cell Differentiation Protein Mcl-1 (MCL1) ,etc. by FLIA (Flow Luminescence Immunoassay) were tested 20 times on one plate, respectively.
Assay procedure summary
1. Preparation of standards, reagents and samples before the experiment
2. Add 100μL standard or sample to each well,
3. Remove liquid on magnetic frame, add 100μL prepared Detection Reagent A. Incubate 60min at 37°
4. Wash plate on magnetic frame for three times
5. Add 100μL prepared Detection Reagent B, and incubate 30 min at 37°
6. Wash plate on magnetic frame for three times
7. Add 100μL sheath solution, swirl for 2 minutes, read on the machine.
C on shaker
C on shaker
C on shaker
add 10μL magnetic beads, and incubate 90min at 37°
1. Preparation of standards, reagents and samples before the experiment
2. Add 100μL standard or sample to each well,
3. Remove liquid on magnetic frame, add 100μL prepared Detection Reagent A. Incubate 60min at 37°
4. Wash plate on magnetic frame for three times
5. Add 100μL prepared Detection Reagent B, and incubate 30 min at 37°
6. Wash plate on magnetic frame for three times
7. Add 100μL sheath solution, swirl for 2 minutes, read on the machine.
C on shaker
C on shaker
C on shaker
add 10μL magnetic beads, and incubate 90min at 37°
UniProt ID
P97287