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AB157723

Mouse SAA ELISA Kit

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(15 Publications)

Mouse SAA ELISA Kit is a sandwich ELISA designed to quantify Mouse SAA with a sensitivity of 10.7 ng/mL.

- Colorimetric sandwich ELISA - 450 nm readout - works on any plate reader
- Wide dynamic range - quantifies 31.25 - 2000 ng/mL
- Cited in over 10 publications

View Alternative Names

Serum amyloid A-1 protein, Saa1

2 Images
Sandwich ELISA - Mouse SAA ELISA Kit (AB157723)
  • sELISA

Supplier Data

Sandwich ELISA - Mouse SAA ELISA Kit (AB157723)

Representative standard curve using ab157723 SAA Mouse ELISA Kit.

Sandwich ELISA - Mouse SAA ELISA Kit (AB157723)
  • sELISA

Lab

Sandwich ELISA - Mouse SAA ELISA Kit (AB157723)

SAA measured in various biological samples showing quantity (ng) per mL of sample tested. For mouse samples (Ms) dilutions of 1 : 1000 were used.

Key facts

Detection method

Colorimetric

Sample types

Plasma, Serum

Reacts with

Mouse

Assay type

Sandwich

Results type

Quantitative

Sensitivity

= 10.7 ng/mL

Range

31.25 - 2000 ng/mL

Assay Platform

Microplate

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "sELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

Product details

Mouse SAA ELISA Kit ab157723 is a sandwich ELISA to measure Mouse SAA in serum, plasma with a sensitivity of 10.7 ng/ml.

How the assay works

In this assay the SAA present in samples reacts with the anti-SAA antibodies which have been adsorbed to the surface of polystyrene microtitre wells. After the removal of unbound proteins by washing, anti-SAA antibodies conjugated with horseradish peroxidase (HRP), are added. These enzyme-labeled antibodies form complexes with the previously bound Serum Amyloid A. Following another washing step, the enzyme bound to the immunosorbent is assayed by the addition of a chromogenic substrate, 3,3',5,5'-tetramethylbenzidine (TMB). The quantity of bound enzyme varies directly with the concentration of SAA in the sample tested; thus, the absorbance, at 450 nm, is a measure of the concentration of Serum Amyloid A in the test sample. The quantity of SAA in the test sample can be interpolated from the standard curve constructed from the standards, and corrected for sample dilution.

Assay Specificity

Our ELISA kits are rigorously validated to ensure the highest level of consistency and reproducibility. Please check the protocol booklet for more details

Mouse SAA ELISA Kit ab157723 protocol summary

1. Add standard or sample to each well used. Incubate at room temperature.
2. Aspirate and wash each well.
3. Add prepared HRP labeled secondary detector antibody. Incubate at room temperature
4. Aspirate and wash each well.
5. Add Chromogen Substrate Solution to each well.
6. Immediately begin recording the color development

Precision

[ { "reproducibilityType": "Intra", "sample": "Overall", "replicates": 0, "mean": null, "standardDeviation": null, "coefficientOfVariability": "< 10" }, { "reproducibilityType": "Inter", "sample": "Overall", "replicates": 0, "mean": null, "standardDeviation": null, "coefficientOfVariability": "< 10" } ]

Recovery

[ { "sample": "Serum", "range": null, "average": "> 85" } ]

What's included?

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Properties and storage information

Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C
Storage information
+4°C

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Serum Amyloid A (SAA) is an important acute-phase protein with a mass of approximately 12 kDa. It plays a role in inflammation and is present in the serum. SAA is an apolipoprotein that associates with high-density lipoprotein (HDL) during inflammatory states. The protein is expressed mainly in the liver and circulating SAA levels greatly increase during inflammatory responses marking it as an important marker for inflammation.
Biological function summary

SAA contributes to the body's immune response to injury by recruiting immune cells and facilitating the removal of cholesterol. As part of the acute-phase response SAA integrates into HDL displacing other apolipoproteins and altering HDL's function. Increased SAA levels can also modulate prostaglandin synthesis and secretion influencing the inflammatory response. The exact role of SAA in pathways beyond these functions continues to be a subject of research.

Pathways

SAA influences lipid metabolism and inflammatory pathways. It plays a significant role within the acute-phase response pathway which modulates the immune system's reaction to stress such as infection or injury. Another pathway involves cholesterol metabolism where SAA interacts with apolipoproteins AI and AII altering the composition and function of HDL particles.

High levels of SAA associate with amyloidosis and chronic inflammatory diseases. In amyloidosis misfolded SAA proteins deposit as amyloid fibrils in tissues leading to organ dysfunction. In dogs and other species SAA is used as a biomarker to monitor inflammatory diseases. Its connection with C-reactive protein further emphasizes its role in inflammatory processes. Research continues to explore how modulating SAA levels may impact disease progression and treatment.

Product protocols

Target data

Major acute phase protein.
See full target information Serum amyloid A-1 protein

Publications (15)

Recent publications for all applications. Explore the full list and refine your search

Cell discovery 10:115 PubMed39557828

2024

Sodium oligomannate disrupts the adherence of Rib bacteria to gut epithelia to block SAA-triggered Th1 inflammation in 5XFAD transgenic mice.

Applications

Unspecified application

Species

Unspecified reactive species

Xinyi Wang,Zuoquan Xie,Jie Yuan,Enjing Jin,Wen Lian,Shuaishuai Chang,Guangqiang Sun,Zhengnan Feng,Hui Xu,Chen Du,Xinying Yang,Aihua Xia,Ji Qiu,Qingli Zhang,Feifei Lin,Jia Liu,Liang Li,Xiaoguang Du,Zhongping Xiao,Zhou Yi,Zhiyu Luo,Changrong Ge,Rui Li,Mingyue Zheng,Yi Jiang,Tao Wang,Jing Zhang,Qihao Guo,Meiyu Geng

Nanotoxicology 15:1295-1311 PubMed35015612

2022

Acute hazard assessment of silver nanoparticles following intratracheal instillation, oral and intravenous injection exposures.

Applications

Unspecified application

Species

Unspecified reactive species

Ali Kermanizadeh,Nicklas R Jacobsen,Agnieszka Mroczko,David Brown,Vicki Stone

Scientific reports 11:14993 PubMed34294791

2021

Periodontitis induces endothelial dysfunction in mice.

Applications

Unspecified application

Species

Unspecified reactive species

Maria Parvaneh,Paul K Witting,Jaqueline Ku,Tala Moradi,Elif Eroglu,Ben Freedman,Greg T Sutherland,Andrew McCorkindale,Boris Guennewig,Phannaphat Choowong,Kim Bell-Anderson,Gregory Cooney,Shane R Thomas,Joerg Eberhard

PLoS neglected tropical diseases 13:e0007515 PubMed31260452

2019

Intestinal parasitic infection alters bone marrow derived dendritic cell inflammatory cytokine production in response to bacterial endotoxin in a diet-dependent manner.

Applications

Unspecified application

Species

Unspecified reactive species

Stacey L Burgess,Akihiko Oka,Bo Liu,David T Bolick,David Noah Oakland,Richard L Guerrant,Luther Bartelt

American journal of physiology. Endocrinology and metabolism 317:E42-E52 PubMed30860877

2019

Human Paneth cell α-defensin-5 treatment reverses dyslipidemia and improves glucoregulatory capacity in diet-induced obese mice.

Applications

Unspecified application

Species

Unspecified reactive species

Ida Søgaard Larsen,Andreas Mæchel Fritzen,Christian Strini Carl,Marianne Agerholm,Mads Thue Fejerskov Damgaard,Jacob Bak Holm,André Marette,Peter Nordkild,Bente Kiens,Karsten Kristiansen,Jan Wehkamp,Benjamin Anderschou Holbech Jensen

Cell 177:399-413.e12 PubMed30853215

2019

Energetic Trade-Offs and Hypometabolic States Promote Disease Tolerance.

Applications

Unspecified application

Species

Unspecified reactive species

Kirthana Ganeshan,Joni Nikkanen,Kevin Man,Yew Ann Leong,Yoshitaka Sogawa,J Alan Maschek,Tyler Van Ry,D Nyasha Chagwedera,James E Cox,Ajay Chawla

EBioMedicine 41:185-199 PubMed30773478

2019

DNA damage repair alterations modulate M2 polarization of microglia to remodel the tumor microenvironment via the p53-mediated MDK expression in glioma.

Applications

Unspecified application

Species

Unspecified reactive species

Xiangqi Meng,Chunbin Duan,Hengyuan Pang,Qun Chen,Bo Han,Caijun Zha,Magafurov Dinislam,Pengfei Wu,Ziwei Li,Shihong Zhao,Ruijia Wang,Lin Lin,Chuanlu Jiang,Jinquan Cai

Arteriosclerosis, thrombosis, and vascular biology 38:1890-1900 PubMed29976766

2018

Serum Amyloid A Is an Exchangeable Apolipoprotein.

Applications

Unspecified application

Species

Unspecified reactive species

Patricia G Wilson,Joel C Thompson,Preetha Shridas,Patrick J McNamara,Maria C de Beer,Frederick C de Beer,Nancy R Webb,Lisa R Tannock

Journal of cellular biochemistry 119:4514-4527 PubMed29236323

2018

Effects of microRNA-330 on vulnerable atherosclerotic plaques formation and vascular endothelial cell proliferation through the WNT signaling pathway in acute coronary syndrome.

Applications

Unspecified application

Species

Unspecified reactive species

Jing Ren,Rui Ma,Zhu-Bo Zhang,Yang Li,Ping Lei,Jian-Long Men

The Journal of nutritional biochemistry 44:52-59 PubMed28399420

2017

Dietary rose hip exerts antiatherosclerotic effects and increases nitric oxide-mediated dilation in ApoE-null mice.

Applications

FuncS

Species

Mouse

Michele Cavalera,Ulrika Axling,Catarina Rippe,Karl Swärd,Cecilia Holm
View all publications
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