The Human IDE (Insulin Degrading Enzyme) ELISA Kit is a highly reliable and accurate tool for the quantification of IDE levels in human samples such as serum, plasma, and cell culture supernatants. With its exceptional sensitivity and specificity, this kit provides consistent and reproducible results, making it an invaluable resource for a variety of research purposes. IDE is a critical enzyme involved in the regulation of insulin levels in the body, playing a key role in glucose metabolism. Dysregulation of IDE has been linked to insulin resistance, diabetes, and other metabolic disorders.
By accurately measuring IDE levels, researchers can gain valuable insights into the mechanisms underlying these conditions and potentially identify new therapeutic targets. This ELISA kit is user-friendly, with clear instructions and step-by-step protocols, allowing for easy and efficient analysis of IDE levels. Whether studying metabolic disorders, exploring potential treatment options, or investigating IDE's broader biological functions, this kit is an essential tool for researchers looking to deepen their understanding of insulin degradation and its impact on human health.
Product Name:
Human IDE/Insulin-degrading enzyme ELISA Kit
SKU:
HUFI01670
Reactivity:
Human
Assay Type:
Sandwich ELISA, Double Antibody
Sensitivity:
37.5 pg/mL
Range:
62.5-4000 pg/mL
Sample Type:
Serum, Plasma, Cell Culture Supernatant, Cell or Tissue Lysate, Other Liquid Samples
Storage:
2-8°C for 12 months.
Linearity:
Sample
1:2
1:4
1:8
Serum (n = 5)
86-104%
83-98%
83-93%
EDTA Plasma (n = 5)
88-104%
90-99%
80-97%
Heparin Plasma (n = 5)
89-105%
87-99%
80-90%
Recovery:
Sample
Recovery Range (%)
Average (%)
Serum (n = 5)
85-102
93
EDTA Plasma (n = 5)
85-101
94
Heparin Plasma (n = 5)
92-102
96
Note:The below protocol is a sample protocol. Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.
Step
Procedure
1
Reagent & Plate Preparation: Equilibrate reagents and TMB substrate to room temperature. Set standard, test sample and control (zero) wells on the pre-coated plate and record their positions.
2
Primary Incubation: Prepare standards, samples, blanks and load into designated wells. Incubate plate at 37°C for 90 minutes to allow antigen binding.
3
Detection Antibody Binding: Add biotin-labeled detection antibody and incubate at 37°C for 60 minutes.
4
HRP-Streptavidin Binding: Add HRP-Streptavidin (SABC) and incubate at 37°C for 30 minutes.
5
Color Development: Add TMB substrate and incubate in the dark for 10–20 minutes.
6
Stop Reaction & Reading: Add stop solution and measure absorbance at 450 nm immediately.
Sample Type
Protocol
Serum
Allow blood to clot, centrifuge at 1000 × g for 20 minutes, collect supernatant supernatant and store appropriately.
Plasma
Collect using anticoagulant tubes, centrifuge at 1000 × g for 15 minutes at 2–8°C and collect plasma.
Tissue Homogenate
Homogenize tissue in PBS with protease inhibitors, centrifuge and collect supernatant.
Cell Culture Supernatant
Centrifuge at 2500 rpm for 5 minutes and collect clarified supernatant.
Cell Lysate
Lyse cells using lysis buffer with protease inhibitors, centrifuge and collect protein supernatant.
Other Sample Types
For more information about how to process other sample types, (e.g., body fluids, breast milk & more), please contact our Tech Support Team at techsupport@assaygenie.com.
Component
Quantity
Storage
48T
96T
ELISA Microplate (Dismountable)
8×6
8×12
Place the test strips into a sealed foil bag with the desiccant. Store for 1 month at 2-8°C; Store for 12 months at -20°C.
Lyophilized Standard
1 vial
2 vial
Place the standards into a sealed foil bag with the desiccant. Store for 1 month at 2-8°C; Store for 12 months at -20°C.
