Comparison

CLIA Kit for Ionized Calcium-binding Adapter Molecule 1 (IBA1)

Item no. SCC288Mu-48T
Manufacturer Cloud-Clone
Amount 48T
Category
Type Elisa-Kit
Specific against Mouse
ECLASS 5.1 32160605
ECLASS 6.1 32160605
ECLASS 8.0 32160605
ECLASS 9.0 32160605
ECLASS 10.0.1 32160605
ECLASS 10.1 32160605
ECLASS 11.0 32160605
UNSPSC 41116126
Alias AIF1, IRT1, Daintain, Protein G1, Allograft Inflammatory Factor 1
Available
Quantity options
Detection range
2.74-2, 000pg/mL
Organism species
Mus musculus (Mouse)
Sensitivity
The minimum detectable dose of this kit is typically less than 0.99pg/mL
Sample type
Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids
Assay length
2h, 40min
Method
Double-antibody Sandwich
Specificity

This assay has high sensitivity and excellent specificity for detection of Ionized Calcium-binding Adapter Molecule 1 (IBA1).
No significant cross-reactivity or interference between Ionized Calcium-binding Adapter Molecule 1 (IBA1) and analogues was observed.

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Ionized Calcium-binding Adapter Molecule 1 (IBA1) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Ionized Calcium-binding Adapter Molecule 1 (IBA1) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

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.

Assay procedure summary
1. Prepare all reagents, samples and standards;
2. Add 100µ L standard or sample to each well. Incubate 2 hours at 37° C;
3. Aspirate and add 100µ L prepared Detection Reagent A. Incubate 1 hour at 37° C;
4. Aspirate and wash 3 times;
5. Add 100µ L prepared Detection Reagent B. Incubate 30 minutes at 37° C;
6. Aspirate and wash 5 times;
7. Add 100µ L Substrate Solution. Incubate 10 minutes at 37° C;
8. Read RLU value immediately.
Test principle
The microplate provided in this kit has been pre-coated with an antibody specific to Ionized Calcium-binding Adapter Molecule 1 (IBA1). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Ionized Calcium-binding Adapter Molecule 1 (IBA1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the Ionized Calcium-binding Adapter Molecule 1 (IBA1) level in the sample or standard.;
Research Area
Cytokine; Infection immunity; Immune molecule;

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 48T
Available: In stock
available

Compare

Add to wishlist

Get an offer

Request delivery time

Ask a technical question

Submit a bulk request

Questions about this Product?
 
Close