The Human Adenosine Deaminase (ADA) ELISA Kit is specifically designed for the precise measurement of ADA levels in human serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit provides accurate and reproducible results, making it an ideal tool for a variety of research applications. Adenosine deaminase is an enzyme that plays a key role in purine metabolism, converting adenosine into inosine. Dysregulation of ADA activity has been linked to immune deficiencies and inflammatory conditions, making it an important biomarker in the study of autoimmune diseases, HIV/AIDS, and certain types of cancer.
By using the Human ADA ELISA Kit, researchers can easily quantify ADA levels in samples, enabling a better understanding of its role in various physiological and pathological processes. Its reliability and precision make it a valuable asset for studies aiming to uncover the mechanisms underlying ADA-related disorders and develop potential therapeutic interventions.
Product Name:
Human Adenosine deaminase/ADA ELISA Kit
SKU:
HUFI01262
Reactivity:
Human
Assay Type:
Sandwich ELISA, Double Antibody
Sensitivity:
0.188 ng/mL
Range:
0.313-20 ng/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)
88-99%
90-103%
97-105%
EDTA Plasma (n = 5)
89-95%
93-100%
82-98%
Heparin Plasma (n = 5)
80-94%
83-100%
84-99%
Recovery:
Sample
Recovery Range (%)
Average (%)
Serum (n = 5)
92-103
99
EDTA Plasma (n = 5)
86-101
95
Heparin Plasma (n = 5)
87-102
97
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.
