Human ADAR (Double-stranded RNA-specific adenosine deaminase) ELISA Kit
The Human ADAR (Double-Stranded RNA Adenosine Deaminase) ELISA Kit is specifically designed for the precise detection of ADAR levels in human samples, including serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring accuracy and reproducibility in results, making it suitable for a wide range of research applications. ADAR is a critical enzyme responsible for converting adenosine to inosine in double-stranded RNA molecules, thereby playing a crucial role in RNA editing and gene expression regulation.
Dysregulation of ADAR has been implicated in various diseases, including cancer, autoimmune disorders, and viral infections, making it a valuable biomarker for understanding these conditions and developing potential therapeutic interventions. Overall, the Human ADAR ELISA Kit provides researchers with a reliable tool for studying ADAR levels in human samples, advancing our understanding of RNA editing mechanisms and their implications in disease pathology.
Product Name:
Human ADAR (Double-stranded RNA-specific adenosine deaminase) ELISA Kit
SKU:
HUFI05467
Reactivity:
Human
Assay Type:
Sandwich ELISA, Double Antibody
Sensitivity:
18.75 pg/mL
Range:
31.25-2000 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)
88-97%
88-99%
82-100%
EDTA Plasma (n = 5)
93-101%
83-97%
89-96%
Heparin Plasma (n = 5)
89-98%
93-100%
82-100%
Recovery:
Sample
Recovery Range (%)
Average (%)
Serum (n = 5)
86-95
91
EDTA Plasma (n = 5)
90-104
95
Heparin Plasma (n = 5)
90-104
98
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.
