The Human CD3D/CD3 Delta ELISA Kit is specifically designed for the quantification of CD3D/CD3 Delta levels in human serum, plasma, and cell culture supernatants. This kit provides highly sensitive and accurate results, ensuring reliable data for a variety of research applications. CD3D/CD3 Delta is a key component of the T-cell receptor complex, playing a critical role in T-cell activation and function. Abnormalities in CD3D/CD3 Delta expression have been linked to various autoimmune diseases, immunodeficiencies, and other immune-related disorders, making it a valuable biomarker for understanding immune system function and disease pathology.
This ELISA kit offers researchers a powerful tool for studying the role of CD3D/CD3 Delta in immune responses and developing potential therapies for immune-related conditions. With its high performance and ease of use, the Human CD3D/CD3 Delta ELISA Kit is an essential addition to any immunology laboratory.
Product Name:
Human CD3d/CD3 delta ELISA Kit
SKU:
HUFI00973
Reactivity:
Human
Assay Type:
Sandwich ELISA, Double Antibody
Sensitivity:
0.094 ng/mL
Range:
0.156-10 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)
86-101%
87-103%
85-104%
EDTA Plasma (n = 5)
83-96%
84-99%
85-96%
Heparin Plasma (n = 5)
82-95%
81-99%
82-99%
Recovery:
Sample
Recovery Range (%)
Average (%)
Serum (n = 5)
93-102
93
EDTA Plasma (n = 5)
88-99
95
Heparin Plasma (n = 5)
89-101
95
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.
Biotin-labeled Antibody (Concentrated, 100X)
60 ul
120 ul
2-8°C (Avoid direct light)
HRP-Streptavidin Conjugate (SABC, 100X)
60 ul
120 ul
2-8°C (Avoid direct light)
TMB Substrate
5 ml
10 ml
2-8°C (Avoid direct light)
Sample Dilution Buffer
10 ml
20 ml
2-8°C
Antibody Dilution Buffer
5 ml
10 ml
2-8°C
SABC Dilution Buffer
5 ml
10 ml
2-8°C
Stop Solution
5 ml
10 ml
2-8°C
Wash Buffer(25X)
15 ml
30 ml
2-8°C
Plate Sealer
3 pieces
5 pieces
-
Technical Manual
1 copy
1 copy
-
Yuan Tao et al.
The value of ACTN1 in the diagnosis of cutaneous squamous cell carcinoma: A continuation study
