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#27191 Human ApoA5 Assay Kit - IBL
- Intended Use:
- Research reagents
- Measuring Method:
- ELISA
- Sample Types:
- Human
- Measuring Samples:
- Serum, EDTA-plasma
- Measurement Range:
- 0.31 - 20 ng/mL
- Package Size1:
- 96 Well
※ The product indicated as "Research reagents" in the column Intended Use cannot be used
for diagnostic nor any medical purpose.
※ The datasheet listed on this page is sample only. Please refer to the datasheet
enclosed in the product purchased before use.
Product Overview
Product Overview
Product Code | 27191 |
---|---|
Product Name | Human ApoA5 Assay Kit - IBL |
Maker Name | Immuno-Biological Laboratories Co., Ltd. |
Intended Use | Research reagents |
Measuring Method | ELISA |
Conjugate | HRP |
Species | Human |
Measuring Samples | Serum, EDTA-plasma |
Measurement Range | 0.31 - 20 ng/mL |
Primary Reaction | 60 minutes at 37 ℃ |
Secondary Reaction | 30 minutes at 2 - 8 ℃ |
Sensitivity | 0.144ng/mL |
Specificity | Substance Cross reactivity (%) ApoA4 ≦0.1 ApoB100 ≦0.1 ApoE2 ≦0.1 ApoE3 ≦0.1 ApoE4 ≦0.1 |
Storage Condition | 2 - 8 ℃ |
Poisonous and Deleterious Substances | Not Applicable |
Cartagena | Not Applicable |
Measuring Service | Available |
Package Size 1 | 96 Well |
Product Description
Product Description
ApoA5 is a protein with 39kDa molecular weight that was discovered by Pennacchio et al. in 2001. It has been reported that ApoA5 is produced in liver and bounds to HDL particles and TG (Triglyceride) rich lipoprotein (CM, VLDL) and exists in blood.
In previous studies, it has been observed that TG level in serum of ApoA5 knockout mice is significantly elevated while it is significantly decreased in serum of the knock-in mice. In addition, since it has been also suggested that ApoA5 deficiency that is caused by ApoA5 gene mutation in human shows severe hypertriglyceridaemia, it has been noted as one of factors of regulating TG metabolism.
This ELISA can specifically measure ApoA5 in human blood.
In previous studies, it has been observed that TG level in serum of ApoA5 knockout mice is significantly elevated while it is significantly decreased in serum of the knock-in mice. In addition, since it has been also suggested that ApoA5 deficiency that is caused by ApoA5 gene mutation in human shows severe hypertriglyceridaemia, it has been noted as one of factors of regulating TG metabolism.
This ELISA can specifically measure ApoA5 in human blood.
References
References
- The Evaluation of Lipid Analysis for PXB-Cells LA as a Human Non-Alcoholic Fatty Liver Disease Model. Masaki Takahashi et al. BPB Reports 2024 Volume 7 Issue 4 Pages 147-156.PMID:
- Influence of apolipoprotein A-V on the metabolic fate of triacylglycerol. Sharma V et al. Curr Opin Lipidol. 2013 Apr;24(2):153-9.PMID: 23241513
- Apolipoprotein A-V dependent modulation of plasma triacylglycerol: a puzzlement. Sharma V et al. Biochim Biophys Acta. 2012 May;1821(5):795-9.PMID: 22209939
- The novel apolipoprotein A5 is present in human serum, is associated with VLDL, HDL, and chylomicrons, and circulates at very low concentrations compared with other apolipoproteins. O'Brien PJ et al. Clin Chem. 2005 Feb;51(2):351-9. Epub 2004 Nov 4.PMID: 15528295
Note: Retrieve by PMID number in displayed by abstract: http://www.ncbi.nlm.nih.gov
FAQ
FAQ
-
Q.What is the immunogen used for the antibodies?
-
A.It is full length recombinant ApoA5.
-
Q.Is composition of EIA buffer of each ELISA kit all same? Can it be mixed to use?
ELISA common FAQ -
A.No it isn't. As constitute of each EIA buffer is different, it cannot be mixed with other lots or EIA buffers contained in other kind of ELISA kits.
-
Q.What is the composition of concentrated wash buffer?
ELISA common FAQ -
A.It contains ordinary Tween and phosphate buffer (0.05% Tween-20 in PB).
-
Q.What is the feature of the plate?
ELISA common FAQ -
A.We use plate that is flat bottom and removable strip type plate (8wellx 12 strips).
-
Q.Can I re-use standard after reconstitution?
ELISA common FAQ -
A.Not recommended to re-use standard after reconstitution. Please use it at once after the reconstitution.
Please note that there are some exceptions. One time freeze-thaw the standard is acceptable for use after reconstitution for some ELISAs.
Please check the details on each product datasheet. -
Q.What is different between reagent blank and test sample blank?
ELISA common FAQ -
A.Reagent blank means a well is only added EIA buffer and the purpose is confirming whether the Test sample value is influenced by lack of washing process or other operations. Test sample blank means a well is added EIA buffer and HRP antibody and the purpose is to calculate the background.
-
Q.How many samples can be measured by this kit?
ELISA common FAQ -
A.The pre-coated plate contained in our ELISA kit is 96 wells plate. We recommend to use 16 wells (2 slits) for standard and 80 wells (10 slits) for 40 samples in duplicate.
-
Q.What is LOD (Limit of Detection)?
ELISA common FAQ -
A.It (LOD) is defined as sensitivity that is calculated using the NCCSL method. Please refer to a datasheet of each product.
-
Q.What is LOQ (Limit of Quantification)?
ELISA common FAQ -
A.It (LOQ) is the lowest value of measurement (standard) range. Please refer to a datasheet of each product.
-
Q.What is the definition of Over Night (O/N) reaction?
ELISA common FAQ -
A.It means that the reaction is required more than 16 hours unless otherwise specifically defined it on a datasheet of each ELISA product.
-
Q.What is the specification of quality control for ELISA product release?
ELISA common FAQ -
A.The information of specification is available on individual lot specific CoA. Please contact us with your reference lot number for obtaining of specific CoA.
-
Q.What is the number (e.g. 432143214321) at the edge of strips of the plate?
ELISA common FAQ -
A.According to the plate maker (ThermoFisher), it does not have any specific meaning as it is just the number of molds.
-
Q.How to wash an ELISA plate?
ELISA common FAQ -
A.Washing it by an auto-washer is highly recommended.
If it is not available, please refer to the demo video (only 2 mins) using a washing bottle. -
Q.The wells turned black during the test with the kit.
ELISA common FAQ -
A.It is possible that the wells were not washed sufficiently during the washing process after the HRP-labeled antibody reaction.
Be sure to wash the wells enough times as described in the data sheet with washing buffer of more than 350 µL.