TAP ELISA kit (Rat)

SKU: CEA634Ra

Size: 96Tests

# of Times Cited in literature: 2

Prepare Time: 2-7 days(please inquire for mutiple units)

Target Name: TAP

Target Full Name: Trypsinogen Activation Peptide

Alternative Names: -

Target Species: Rat

Uniprot: P00763 & P00762

Gene ID: 25052 & 24691

Featured Series: CE kit

Featured Series Function: Detects small molecule

Specificity: Reactive with Rat TAP / Trypsinogen Activation Peptide

Method: Colormetric

Detection principle: Competitive Inhibition

Detection range: 123.5-10,000pg/mL

Sensitivity: 50.3pg/mL

Assay Time: 2h

Sample Size: 50uL

Recommended/Predicted Sample Types: Serum, Plasma, Tissue Homogenates, Cell Lysates, Cell Culture Supernates and other Biological Fluids

Assay Precision: Intra-Assay: CV<10%, Inter-Assay: CV<12%

Reproducibility test menthod: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Trypsinogen Activation Peptide (TAP) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Trypsinogen Activation Peptide (TAP) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100

Storage: 4°C for 1 month/ -20°C for long-term(One year within shelf life)

Shelf-life: 12 months

Specificity: This assay has high sensitivity and excellent specificity for detection of Trypsinogen Activation Peptide (TAP). No significant cross-reactivity or interference between Trypsinogen Activation Peptide (TAP) and analogues was observed.

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 50µL standard or sample to each well. And then add 50µL prepared Detection Reagent A immediately. Shake and mix. Incubate 1 hour at 37°C; 3. Aspirate and wash 3 times; 4. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C; 5. Aspirate and wash 5 times; 6. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C; 7. Add 50µL Stop Solution. Read at 450 nm immediately.

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Trypsinogen Activation Peptide (TAP) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Trypsinogen Activation Peptide (TAP) and unlabeled Trypsinogen Activation Peptide (TAP) (Standards or samples) with the pre-coated antibody specific to Trypsinogen Activation Peptide (TAP). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Trypsinogen Activation Peptide (TAP) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Trypsinogen Activation Peptide (TAP) in the sample.

Research Area: Infection immunity;Immune molecule;Hepatology;

References Citing This Product: Prior peritoneal lavage with hot 0.9% saline induces HSP70 expression and protects against cerulein-induced acute pancreatitis in rats

Effects of Calcium Channel Blockers on Trypsinogen Activation and Severity of Cerulein-induced Acute Pancreatitis in Rats

Investigation of non-pharmaceutical cures for acute pancreatitis induced by cerulein in rats

The Regulatory Effect of the Kinase Inhibitor PD98059 on Autophagic Flux During Trypsinogen Activation in Pancreatic Acinar Cells