추천 제품
종 반응성
human
제조업체/상표
Milliplex®
assay range
accuracy: 95-96%
standard curve range: 10-40,000 pg/mL
(for COMP)
standard curve range: 2-10,000 pg/mL
(for IL-18BPa)
standard curve range: 6-25,000 pg/mL
(for Uteroglobin)
inter-assay cv: <20%
intra-assay cv: <10%
기술
multiplexing: suitable
검출 방법
fluorometric (Luminex® xMAP®)
배송 상태
wet ice
저장 온도
2-8°C
일반 설명
Fibrosis is a pathological wound healing response that is common to many chronic diseases and injuries. The abnormal wound healing response of fibrosis involves the excessive accumulation of the extracellular matrix components responsible for the formation of scar tissue. Progressive tissue scarring causes alterations to normal organ structure leading to dysfunction and failure. Fibrosis and related diseases are responsible for an increasing burden of morbidity and mortality worldwide. This panel of fibrosis-related biomarkers enables researchers to advance understanding of the complex processes associated with fibrotic diseases, including but not limited to idiopathic pulmonary fibrosis, liver fibrosis, and lung fibrosis.
Our MILLIPLEX® Human Fibrosis Panel 1 is a 3-plex kit to be used for the simultaneous quantification of any or all of the following analytes in serum, plasma and tissue culture samples:
IL-18 Binding Protein A (IL-18BPa), Cartilage Oligomeric Matrix Protein (COMP), and Uteroglobin.
MILLIPLEX® offers the broadest selection of analytes across a wide range of disease states and species. Once the analytes of interest have been identified, you can rely on the quality that we build into each kit to produce results you can trust. In addition to the assay characteristics listed in the protocol, other performance criteria evaluated during the verification process include: cross-reactivity, dilution linearity, kit stability, and sample behavior (e.g. detectability and stability).
Each MILLIPLEX® panel and kit includes:
In addition each panel and kit meets stringent manufacturing criteria to ensure batch-to-batch reproducibility. The MILLIPLEX® Human Fibrosis Panel 1 thus enables you to focus on the therapeutic potential of cytokines and the modulation of cytokine expression. Coupled with the Luminex® xMAP® platform in a magnetic bead format, you receive the advantage of ideal speed and sensitivity, allowing quantitative multiplex detection of dozens of analytes simultaneously, which can dramatically improve productivity.
Our MILLIPLEX® Human Fibrosis Panel 1 is a 3-plex kit to be used for the simultaneous quantification of any or all of the following analytes in serum, plasma and tissue culture samples:
IL-18 Binding Protein A (IL-18BPa), Cartilage Oligomeric Matrix Protein (COMP), and Uteroglobin.
MILLIPLEX® offers the broadest selection of analytes across a wide range of disease states and species. Once the analytes of interest have been identified, you can rely on the quality that we build into each kit to produce results you can trust. In addition to the assay characteristics listed in the protocol, other performance criteria evaluated during the verification process include: cross-reactivity, dilution linearity, kit stability, and sample behavior (e.g. detectability and stability).
Each MILLIPLEX® panel and kit includes:
- Quality controls (QCs) to qualify assay performance
- Comparison of standard (calibrator) and QC lots to a reference lot to ensure lot-to-lot consistency
- Optimized serum matrix to mimic native analyte environment in serum and plasma samples
- Detection antibody cocktails designed to yield consistent analyte profiles within panel
In addition each panel and kit meets stringent manufacturing criteria to ensure batch-to-batch reproducibility. The MILLIPLEX® Human Fibrosis Panel 1 thus enables you to focus on the therapeutic potential of cytokines and the modulation of cytokine expression. Coupled with the Luminex® xMAP® platform in a magnetic bead format, you receive the advantage of ideal speed and sensitivity, allowing quantitative multiplex detection of dozens of analytes simultaneously, which can dramatically improve productivity.
특이성
Cross Reactivity:
Negligible or no cross-reactivity was observed between the antibodies for any one analyte and any of the other analytes in this panel.
Negligible or no cross-reactivity was observed between the antibodies for any one analyte and any of the other analytes in this panel.
애플리케이션
The Human Fibrosis Panel 1, using the Luminex® xMAP® technology, enables simultaneous quantification of 3 fibrosis protein biomarkers in human serum, plasma and tissue/cell culture samples.
Researchers will need access to a Luminex® 200, MAGPIX, or FLEXMAP 3D instrument.
Analytes Available:
Research Category:
Research Sub-Category:
- This assay may be run overnight (16-18 hours) at 2-8°C or for 2 hours at room temperature (20-25°C) with agitation on a plate shaker.
- A maximum of 25 μL per well of 1:200 serum or plasma diluted in Assay Buffer should be used for all analytes. Tissue culture supernatants may require dilution in appropriate control medium.
- Tissue/cell extracts should be prepared in neutral buffers containing reagents and conditions that do not interfere with assay performance.
Researchers will need access to a Luminex® 200, MAGPIX, or FLEXMAP 3D instrument.
Analytes Available:
- COMP
- IL-18BPa
- Uteroglobin
Research Category:
- Inflammation & Immunology
Research Sub-Category:
- Inflammation & Autoimmune Mechanisms
- Inflammation
- Infectious Diseases
- Cytokines & Cytokine Receptors
- Growth Factors & Receptors
- Oncology
- Obesity
- Metabolic Disorders
- Autoimmune disease
- Cardiovascular Disease
특징 및 장점
Configuration:
Design your multiplex kit by choosing available analytes within this panel.
Design your multiplex kit by choosing available analytes within this panel.
포장
96 well plate
법적 정보
Luminex is a registered trademark of Luminex Corp
MILLIPLEX is a registered trademark of Merck KGaA, Darmstadt, Germany
xMAP is a registered trademark of Luminex Corp
면책조항
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Sens. 1 - STOT RE 2
표적 기관
Respiratory Tract
Storage Class Code
10 - Combustible liquids
시험 성적서(COA)
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