The Human TPD52 (Tumor Protein D52) ELISA Kit is a reliable and accurate tool for the detection of TPD52 levels in human serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit delivers dependable and reproducible results, making it a valuable asset for various research applications. TPD52 is a protein that plays a crucial role in cancer progression and metastasis, making it a promising biomarker for cancer research and treatment development.
By measuring TPD52 levels, researchers can gain valuable insights into tumor growth and potentially identify new therapeutic targets. Overall, the Human TPD52 ELISA Kit offers researchers a powerful tool for studying the role of TPD52 in cancer and other related diseases, ultimately paving the way for new advancements in cancer diagnostics and treatment.
Product Name:
Human TPD52/Tumor protein D52 ELISA Kit
SKU:
HUFI01196
Reactivity:
Human
Assay Type:
Competitive ELISA, Coated with Antigen
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(Sealed), Don't cryopreserve.
Linearity:
Sample
1:2
1:4
1:8
Serum (n = 10)
86-102%
93-105%
85-105%
EDTA Plasma (n = 10)
86-98%
90-99%
86-101%
Heparin Plasma (n = 10)
82-98%
81-98%
81-99%
Recovery:
Sample
Recovery Range (%)
Average (%)
Serum (n = 10)
86-96
91
EDTA Plasma (n = 10)
90-103
95
Heparin Plasma (n = 10)
89-105
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 TMB substrate for 30 minutes at room temperature. Prepare standards, samples (minimum 1:2 dilution), blanks, assign wells, and pre-wash the plate twice.
2
Sample & Biotin-Antibody Binding: Add 50 µL standard or sample followed by 50 µL biotin-labeled antibody to each well. Mix gently and incubate at 37°C for 45 minutes.
3
Washing: Wash the plate 5 times with wash buffer, allowing 1 minute soak time per wash.
4
Color Development: Add TMB substrate and incubate in the dark at 37°C for 10-20 minutes until color develops.
5
Stop Reaction: Add stop solution to terminate the reaction. The color changes from blue to yellow immediately.
6
Reading: Measure absorbance at 450 nm using a microplate reader.
Sample Type
Protocol
Serum
Allow blood to clot, centrifuge at 1000 × g for 20 minutes, collect supernatant and store appropriately.
Plasma
Collect using EDTA anticoagulant, centrifuge at 1000 × g for 15 minutes at 2–8°C and collect plasma.
Cell Culture Supernatant
Centrifuge at 1000 × g for 20 minutes at 4°C and collect clarified supernatant.
Cell Lysate
Lyse cells using recommended lysis buffer with protease inhibitors, centrifuge at 10,000 rpm for 10 minutes, and collect protein supernatant.
Tissue Homogenate
Homogenize tissue in PBS with protease inhibitors, centrifuge at 5000 × g for 5 minutes, and collect supernatant.
Other Sample Types
Centrifuge samples at 1000 × g for 15 minutes at 2–8°C and collect supernatant. For additional guidance, please contact 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.
