Human ApoC1 (Apolipoprotein C1) ELISA Kit (HUES01670)
- SKU:
- HUES01670
- Product Type:
- ELISA Kit
- Size:
- 96 Assays
- Uniprot:
- P02654
- Sensitivity:
- 5.63ng/mL
- Range:
- 9.38-600ng/mL
- ELISA Type:
- Sandwich
- Synonyms:
- Apolipoprotein C-I, Apolipoprotein C1, APOC1, apo-CIB, apoC-IB,
- Reactivity:
- Human
- Sample Type:
- Serum, plasma and other biological fluids
- Research Area:
- Cell Biology
Description
Human ApoC1 (Apolipoprotein C1) ELISA Kit
The Human APOC1 (Apolipoprotein C1) ELISA Kit is specifically designed for the precise quantification of apolipoprotein C1 levels in human serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring consistent and accurate results for a variety of research applications.Apolipoprotein C1 is a critical component involved in lipid metabolism and cardiovascular health. It plays a key role in regulating plasma lipid levels and is associated with conditions such as dyslipidemia, atherosclerosis, and cardiovascular disease.
Monitoring apolipoprotein C1 levels can provide valuable insights into these conditions and aid in the development of potential therapies.Overall, the Human APOC1 ELISA Kit is a valuable tool for researchers interested in studying lipid metabolism, cardiovascular health, and related disorders. Its high quality and reliability make it an essential part of any laboratory focusing on these areas of research.
Assay type: | Sandwich |
Format: | 96T |
Assay time: | 4.5h |
Reactivity: | Human |
Detection Method: | Colormetric |
Detection Range: | 9.38-600 ng/mL |
Sensitivity: | 5.63 ng/mL |
Sample Volume Required Per Well: | 100µL |
Sample Type: | Serum, plasma and other biological fluids |
Specificity: | This kit recognizes Human ApoC1 in samples. No significant cross-reactivity or interference between Human ApoC1 and analogues was observed. |
This ELISA kit uses Sandwich-ELISA as the method. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Human ApoC1. Standards or samples are added to the appropriate micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Human ApoC1 and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well successively and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Human ApoC1, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by adding Stop Solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Human ApoC1. The concentration of Human ApoC1 in samples can be calculated by comparing the OD of the samples to the standard curve.
UniProt Protein Function: | APOC1: Appears to modulate the interaction of APOE with beta- migrating VLDL and inhibit binding of beta-VLDL to the LDL receptor-related protein. Binds free fatty acids and reduces their intracellular esterification. Belongs to the apolipoprotein C1 family. |
UniProt Protein Details: | Protein type:Secreted, signal peptide; Lipid-binding; Secreted; Inhibitor; Endoplasmic reticulum Chromosomal Location of Human Ortholog: 19q13. 2 Cellular Component: chylomicron; endoplasmic reticulum Molecular Function:phospholipase inhibitor activity; lipase inhibitor activity; phosphatidylcholine binding; fatty acid binding Biological Process: positive regulation of catalytic activity; cholesterol metabolic process; triacylglycerol metabolic process; phospholipid efflux; negative regulation of lipid catabolic process; negative regulation of cholesterol transport; negative regulation of lipoprotein lipase activity; cholesterol efflux; lipoprotein metabolic process; negative regulation of receptor-mediated endocytosis; lipid metabolic process; negative regulation of lipid metabolic process; regulation of cholesterol transport; negative regulation of fatty acid biosynthetic process |
NCBI Summary: | The protein encoded by this gene is a member of the apolipoprotein C1 family. This gene is expressed primarily in the liver, and it is activated when monocytes differentiate into macrophages. A pseudogene of this gene is located 4 kb downstream in the same orientation, on the same chromosome. This gene is mapped to chromosome 19, where it resides within a apolipoprotein gene cluster. Alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008] |
UniProt Code: | P02654 |
NCBI GenInfo Identifier: | 114016 |
NCBI Gene ID: | 341 |
NCBI Accession: | P02654. 1 |
UniProt Secondary Accession: | P02654,Q6IB97, B2R526, |
UniProt Related Accession: | P02654 |
Molecular Weight: | 83 |
NCBI Full Name: | Apolipoprotein C-I |
NCBI Synonym Full Names: | apolipoprotein C-I |
NCBI Official Symbol: | APOC1 |
NCBI Official Synonym Symbols: | Apo-CI; ApoC-I |
NCBI Protein Information: | apolipoprotein C-I; apo-CIB; apoC-IB; apolipoprotein C1; apolipoprotein C-I variant I |
UniProt Protein Name: | Apolipoprotein C-I |
UniProt Synonym Protein Names: | Apolipoprotein C1Truncated apolipoprotein C-I |
Protein Family: | Apolipoprotein |
UniProt Gene Name: | APOC1 |
UniProt Entry Name: | APOC1_HUMAN |
As the OD values of the standard curve may vary according to the conditions of the actual assay performance (e. g. operator, pipetting technique, washing technique or temperature effects), the operator should establish a standard curve for each test. Typical standard curve and data is provided below for reference only.
Concentration (ng/mL) | O.D | Average | Corrected |
600 | 2.34 2.4 | 2.37 | 2.314 |
300 | 1.64 1.654 | 1.647 | 1.591 |
150 | 0.984 0.968 | 0.976 | 0.92 |
75 | 0.459 0.499 | 0.479 | 0.423 |
37.5 | 0.277 0.265 | 0.271 | 0.215 |
18.75 | 0.16 0.156 | 0.158 | 0.102 |
9.38 | 0.104 0.112 | 0.108 | 0.052 |
0 | 0.054 0.058 | 0.056 | -- |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Human ApoC1 were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Human ApoC1 were tested on 3 different plates, 20 replicates in each plate.
Intra-assay Precision | Inter-assay Precision | |||||
Sample | 1 | 2 | 3 | 1 | 2 | 3 |
n | 20 | 20 | 20 | 20 | 20 | 20 |
Mean (ng/mL) | 28.50 | 51.80 | 289.30 | 26.30 | 46.60 | 294.50 |
Standard deviation | 1.70 | 2.90 | 10.40 | 1.40 | 2.10 | 11.50 |
C V (%) | 5.96 | 5.60 | 3.59 | 5.32 | 4.51 | 3.90 |
Recovery
The recovery of Human ApoC1 spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.
Sample Type | Range (%) | Average Recovery (%) |
Serum (n=5) | 86-102 | 93 |
EDTA plasma (n=5) | 93-108 | 99 |
Cell culture media (n=5) | 86-100 | 92 |
Linearity
Samples were spiked with high concentrations of Human ApoC1 and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.
Serum (n=5) | EDTA plasma (n=5) | Cell culture media (n=5) | ||
1:2 | Range (%) | 85-97 | 92-108 | 98-114 |
Average (%) | 91 | 99 | 105 | |
1:4 | Range (%) | 99-114 | 83-98 | 96-109 |
Average (%) | 107 | 89 | 102 | |
1:8 | Range (%) | 99-115 | 87-98 | 96-109 |
Average (%) | 105 | 93 | 102 | |
1:16 | Range (%) | 102-115 | 84-97 | 92-105 |
Average (%) | 107 | 89 | 98 |
An unopened kit can be stored at 4°C for 1 month. If the kit is not used within 1 month, store the items separately according to the following conditions once the kit is received.
Item | Specifications | Storage |
Micro ELISA Plate(Dismountable) | 8 wells ×12 strips | -20°C, 6 months |
Reference Standard | 2 vials | |
Concentrated Biotinylated Detection Ab (100×) | 1 vial, 120 µL | |
Concentrated HRP Conjugate (100×) | 1 vial, 120 µL | -20°C(shading light), 6 months |
Reference Standard & Sample Diluent | 1 vial, 20 mL | 4°C, 6 months |
Biotinylated Detection Ab Diluent | 1 vial, 14 mL | |
HRP Conjugate Diluent | 1 vial, 14 mL | |
Concentrated Wash Buffer (25×) | 1 vial, 30 mL | |
Substrate Reagent | 1 vial, 10 mL | 4°C(shading light) |
Stop Solution | 1 vial, 10 mL | 4°C |
Plate Sealer | 5 pieces | |
Product Description | 1 copy | |
Certificate of Analysis | 1 copy |
- Set standard, test sample and control (zero) wells on the pre-coated plate and record theirpositions. It is recommended to measure each standard and sample in duplicate. Note: addall solutions to the bottom of the plate wells while avoiding contact with the well walls. Ensuresolutions do not foam when adding to the wells.
- Aliquot 100 µL of standard solutions into the standard wells.
- Add 100 µL of Sample / Standard dilution buffer into the control (zero) well.
- Add 100 µL of properly diluted sample (serum, plasma, tissue homogenates and otherbiological fluids) into test sample wells.
- Cover the plate with the sealer provided in the kit and incubate for 90 min at 37 °C.
- Aspirate the liquid from each well, do not wash. Immediately add 100 µL of BiotinylatedDetection Ab working solution to each well. Cover the plate with a plate seal and gently mix. Incubate for 1 hour at 37 °C.
- Aspirate or decant the solution from the plate and add 350 µL of wash buffer to each welland incubate for 1-2 minutes at room temperature. Aspirate the solution from each well andclap the plate on absorbent filter paper to dry. Repeat this process 3 times. Note: a microplatewasher can be used in this step and other wash steps.
- Add 100 µL of HRP Conjugate working solution to each well. Cover with a plate seal andincubate for 30 min at 37 °C.
- Aspirate or decant the solution from each well. Repeat the wash process for five times asconducted in step 7.
- Add 90 µL of Substrate Reagent to each well. Cover with a new plate seal and incubate forapproximately 15 min at 37 °C. Protect the plate from light. Note: the reaction time can beshortened or extended according to the actual color change, but not by more than 30min.
- Add 50 µL of Stop Solution to each well. Note: Adding the stop solution should be done inthe same order as the substrate solution.
- Determine the optical density (OD value) of each well immediately with a microplate readerset at 450 nm.