LBP ELISA Kit

Catalog No. ABIN414694

Product Details LBP ELISA Kit

Target: LBP (Lipopolysaccharide Binding Protein (LBP))

Reactivity: Human

Detection Method: Colorimetric

Method Type: Sandwich ELISA

Detection Range: 3.12 ng/mL - 200 ng/mL

Minimum Detection Limit: 3.12 ng/mL

Application: ELISA

Purpose: The kit is a sandwich enzyme immunoassay for in vitro quantitative measurement of LBP in Serum,Plasma,Biological Fluids

Sample Type: Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate

Analytical Method: Quantitative

Specificity:

This assay has high sensitivity and excellent specificity for detection of Lipopolysaccharide Binding Protein (LBP).
No significant cross-reactivity or interference between Lipopolysaccharide Binding Protein (LBP) and analogues was observed.

Cross-Reactivity (Details): No significant cross-reactivity or interference between Lipopolysaccharide Binding Protein (LBP) and analogues was observed.

Sensitivity: 1.21 ng/mL

Components:

• Pre-coated, ready to use 96-well strip plate, flat buttom
• Plate sealer for 96 wells
• Reference Standard
• Standard Diluent
• Detection Reagent A
• Detection Reagent B
• Assay Diluent A
• Assay Diluent B
• Reagent Diluent (if Detection Reagent is lyophilized)
• TMB Substrate
• Stop Solution
• Wash Buffer (30 x concentrate)
• Instruction manual

Application Details

Application Notes:

• Limited by the current condition and scientific technology, we cannot completely conduct the comprehensive identification and analysis on the raw material provided by suppliers. So there might be some qualitative and technical risks to use the kit.
• The final experimental results will be closely related to validity of the products, operation skills of the end users and the experimental environments. Please make sure that sufficient samples are available.
• Kits from different batches may be a little different in detection range, sensitivity and color developing time.
• Do not mix or substitute reagents from one kit lot to another. Use only the reagents supplied by manufacturer.
• Protect all reagents from strong light during storage and incubation. All the bottle caps of reagents should be covered tightly to prevent the evaporation and contamination of microorganism.
• There may be some foggy substance in the wells when the plate is opened at the first time. It will not have any effect on the final assay results. Do not remove microtiter plate from the storage bag until needed.
• Wrong operations during the reagents preparation and loading, as well as incorrect parameter setting for the plate reader may lead to incorrect results. A microplate plate reader with a bandwidth of 10nm or less and an optical density range of 0-3 O.D. or greater at 450 ± 10nm wavelength is acceptable for use in absorbance measurement. Please read the instruction carefully and adjust the instrument prior to the experiment.
• Even the same operator might get different results in two separate experiments. In order to get better reproducible results, the operation of every step in the assay should be controlled. Furthermore, a preliminary experiment before assay for each batch is recommended.
• Each kit has been strictly passed Q.C test. However, results from end users might be inconsistent with our in-house data due to some unexpected transportation conditions or different lab equipments. Intra-assay variance among kits from different batches might arise from above factors, too.
• Kits from different manufacturers for the same item might produce different results, since we have not compared our products with other manufacturers.

Comment:

Information on standard material:
The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

Information on reagents:
The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

Information on antibodies:
The provided antibodies and their host vary in different kits.

Sample Volume: 100 μL

Assay Time: 3 h

Plate: Pre-coated

Protocol: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Lipopolysaccharide Binding Protein (LBP). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Lipopolysaccharide Binding Protein (LBP). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Lipopolysaccharide Binding Protein (LBP), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Lipopolysaccharide Binding Protein (LBP) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Reagent Preparation:

1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
2. Standard - Reconstitute the Standard with 0.5 mL of Standard Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). The concentration of the standard in the stock solution is 200 ng/mL. Prepare 7 tubes containing 0.25 mL Standard Diluent and produce a double dilution series. Mix each tube thoroughly before the next transfer. Set up 7 points of diluted standard such as 200 ng/mL, 100 ng/mL, 50 ng/mL, 25 ng/mL, 12.5 ng/mL, 6.25 ng/mL, 3.12 ng/mL, and the last microcentrifuge tube with Standard Diluent is the blank as 0 ng/mL.
3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, keep for 10 minutes at room temperature, shake gently (not to foam). Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
4. Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
5. TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.

Note:

1. Making serial dilution in the wells directly is not permitted.
2. Prepare standards within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
3. Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10μL for one pipetting.
4. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
5. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
6. Contaminated water or container for reagent preparation will influence the detection result.

Assay Precision:

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Lipopolysaccharide Binding Protein (LBP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Lipopolysaccharide Binding Protein (LBP) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Restrictions: For Research Use only

Handling

Precaution of Use: The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.

Handling Advice: The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

Storage: 4 °C

Storage Comment:

• For unopened kit: All the reagents should be kept according to the labels on vials. The Standard, Detection Reagent A, Detection Reagent B and the 96-well strip plate should be stored at -20°C upon receipt while the others should be at 4°C.
• For opened kit: When the kit is opened, the remaining reagents still need to be stored according to the above storage condition. Besides, please return the unused wells to the foil pouch containing the desiccant pack, and reseal along entire edge of zip-seal.
  Note: It is highly recommended to use the remaining reagents within 1 month provided this is within the expiration date of the kit.
• For ELISA kit, 1 day storage at 37°C can be considered as 2 months at 4°C, which means 3 days at 37°C equaling 6 months at 4°C.

Expiry Date: 6 months

References for LBP ELISA Kit (ABIN414694)

Tenorio-Jiménez, Martínez-Ramírez, Del Castillo-Codes, Arraiza-Irigoyen, Tercero-Lozano, Camacho, Chueca, García, Olza, Plaza-Díaz, Fontana, Olivares, Gil, Gómez-Llorente: "Lactobacillus reuteri V3401 Reduces Inflammatory Biomarkers and Modifies the Gastrointestinal Microbiome in Adults with Metabolic Syndrome: The PROSIR Study." in: Nutrients, Vol. 11, Issue 8, (2020) (PubMed).

Tenorio-Jiménez, Martínez-Ramírez, Tercero-Lozano, Arraiza-Irigoyen, Del Castillo-Codes, Olza, Plaza-Díaz, Fontana, Migueles, Olivares, Gil, Gomez-Llorente et al.: "Evaluation of the effect of Lactobacillus reuteri V3401 on biomarkers of inflammation, cardiovascular risk and liver steatosis in obese adults with metabolic syndrome: a randomized clinical trial ..." in: BMC complementary and alternative medicine, Vol. 18, Issue 1, pp. 306, (2019) (PubMed).

Kim, Kim, Jeong, Kim, Choi, Chae, Kwon: "A standardized extract of the fruit of Hovenia dulcis alleviated alcohol-induced hangover in healthy subjects with heterozygous ALDH2: A randomized, controlled, crossover trial." in: Journal of ethnopharmacology, Vol. 209, pp. 167-174, (2018) (PubMed).

Kaltsa, Bamias, Siakavellas, Goukos, Karagiannakis, Zampeli, Vlachogiannakos, Michopoulos, Vafiadi, Daikos, Ladas: "Systemic levels of human β-defensin 1 are elevated in patients with cirrhosis." in: Annals of gastroenterology : quarterly publication of the Hellenic Society of Gastroenterology, Vol. 29, Issue 1, pp. 63-70, (2016) (PubMed).

Agiasotelli, Alexopoulou, Vasilieva, Hadziyannis, Goukos, Daikos, Dourakis: "High serum lipopolysaccharide binding protein is associated with increased mortality in patients with decompensated cirrhosis." in: Liver international : official journal of the International Association for the Study of the Liver, Vol. 37, Issue 4, pp. 576-582, (2016) (PubMed).

Upur, Chen, Kamilijiang, Deng, Sulaiman, Aizezi, Wu, Tulake, Abudula: "Identification of plasma protein markers common to patients with malignant tumour and Abnormal Savda in Uighur medicine: a prospective clinical study." in: BMC complementary and alternative medicine, Vol. 15, pp. 9, (2015) (PubMed).

Xiao, Fei, Pang, Shen, Wang, Zhang, Zhang, Zhang, Zhang, Li, Sun, Xue, Wang, Feng, Yan, Zhao, Liu, Long, Zhao: "A gut microbiota-targeted dietary intervention for amelioration of chronic inflammation underlying metabolic syndrome." in: FEMS microbiology ecology, Vol. 87, Issue 2, pp. 357-67, (2014) (PubMed).

Jialal, Rajamani, Adams-Huet, Kaur: "Circulating pathogen-associated molecular pattern - binding proteins and High Mobility Group Box protein 1 in nascent metabolic syndrome: implications for cellular Toll-like receptor activity." in: Atherosclerosis, Vol. 236, Issue 1, pp. 182-7, (2014) (PubMed).

Asmuth, Ma, Albanese, Sandler, Devaraj, Knight, Flynn, Yotter, Garcia, Tsuchida, Wu, Douek, Miller: "Oral serum-derived bovine immunoglobulin improves duodenal immune reconstitution and absorption function in patients with HIV enteropathy." in: AIDS, Vol. 27, Issue 14, pp. 2207-17, (2013) (PubMed).

Martínez, Lattimer, Hubach, Case, Yang, Weber, Louk, Rose, Kyureghian, Peterson, Haub, Walter: "Gut microbiome composition is linked to whole grain-induced immunological improvements." in: The ISME journal, Vol. 7, Issue 2, pp. 269-80, (2013) (PubMed).

Papadopoulos, Bakhtiary, Grün, Weber, Strasser, Moritz: "The effect of normovolemic modified ultrafiltration on inflammatory mediators, endotoxins, terminal complement complexes and clinical outcome in high-risk cardiac surgery patients." in: Perfusion, Vol. 28, Issue 4, pp. 306-14, (2013) (PubMed).

Karagiannakis, Vlachogiannakos, Anastasiadis, Vafiadis-Zouboulis, Ladas: "Frequency and severity of cirrhotic cardiomyopathy and its possible relationship with bacterial endotoxemia." in: Digestive diseases and sciences, Vol. 58, Issue 10, pp. 3029-36, (2013) (PubMed).

Sun, Yu, Ye, Zou, Li, Yu, Wu, Chen, Dore, Clément, Hu, Lin: "A marker of endotoxemia is associated with obesity and related metabolic disorders in apparently healthy Chinese." in: Diabetes Care, Vol. 33, Issue 9, pp. 1925-32, (2010) (PubMed).

Sunni, Bishop, Kent, Geer: "Diabetic cardiomyopathy. A morphological study of intramyocardial arteries." in: Archives of pathology & laboratory medicine, Vol. 110, Issue 5, pp. 375-81, (1986) (PubMed).

Target Details for LBP

Target: LBP (Lipopolysaccharide Binding Protein (LBP))

Alternative Name: LBP (LBP Products)

Synonyms: BPIFD2 ELISA Kit, Bpifd2 ELISA Kit, Ly88 ELISA Kit, LPSBP ELISA Kit, LBP ELISA Kit, lipopolysaccharide binding protein ELISA Kit, lipopolysaccharide-binding protein ELISA Kit, LBP ELISA Kit, Lbp ELISA Kit, LOC100472839 ELISA Kit

UniProt: P18428

Pathways: TLR Signaling, Activation of Innate immune Response, Cellular Response to Molecule of Bacterial Origin, Positive Regulation of Immune Effector Process, Toll-Like Receptors Cascades, Monocarboxylic Acid Catabolic Process