Recombinant Mouse Serum Amyloid A1 Protein, CF

Catalog # Availability Size / Price Qty
2948-SA-025
R&D Systems Recombinant Proteins and Enzymes
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Citations (4)
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Recombinant Mouse Serum Amyloid A1 Protein, CF Summary

Product Specifications

Purity
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining.
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method.
Activity
Measured by its ability to induce TNF-alpha secretion by J774A.1 mouse reticulum cell sarcoma macrophage cells.

The ED50 for this effect is 1.5-7.5 μg/mL.

Source
E. coli-derived mouse Serum Amyloid A1 protein
Gly20-Tyr122
Accession #
N-terminal Sequence
Analysis
Gly20
Predicted Molecular Mass
11.8 kDa
SDS-PAGE
11 kDa, reducing conditions

Product Datasheets

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2948-SA

Carrier Free

What does CF mean?

CF stands for Carrier Free (CF). We typically add Bovine Serum Albumin (BSA) as a carrier protein to our recombinant proteins. Adding a carrier protein enhances protein stability, increases shelf-life, and allows the recombinant protein to be stored at a more dilute concentration. The carrier free version does not contain BSA.

What formulation is right for me?

In general, we advise purchasing the recombinant protein with BSA for use in cell or tissue culture, or as an ELISA standard. In contrast, the carrier free protein is recommended for applications, in which the presence of BSA could interfere.

2948-SA

Formulation Lyophilized from a 0.2 μm filtered solution in Tris-HCl, NaCl, PEG and Imidazole.
Reconstitution Reconstitute at 100 μg/mL in PBS.
Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 1 month, 2 to 8 °C under sterile conditions after reconstitution.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
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Reconstitution Calculator

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Background: Serum Amyloid A1

Mouse Serum Amyloid A protein‑1 (SAA1; previously SAA2 in mouse) is a multifunctional apolipoprotein produced by hepatocytes in response to pro‑inflammatory cytokines (1 ‑ 4). It is secreted as a 12 kDa, 103 amino acid (aa), nonglycosylated protein and circulates as part of the HDL complex (1 ‑ 4). The SAA1 gene is one of five SAA genes in mouse (3). Mature mouse SAA1 shares 72%, 72% and 67% amino acid (aa) sequence identity with human, rabbit and equine SAA1, respectively. SAA1 and SAA2 share 113 of their 122 amino acids and are termed A‑SAA (acute phase SAA) (2, 3). SAA1 is produced in the liver in both human and mouse (3, 4). SAA1 is prominently produced in human adipose tissue, but is absent in mouse adipose, which instead expresses adipose SAA3 (a pseudogene in humans) (5). In mouse, however, circulating SAA1 is elevated by insulin resistance (6). A‑SAA can increase by as much as 1000‑fold during inflammation (3). When highly expressed, A‑SAA can displace ApoA1 as the major apolipoprotein in HDL complexes, weakening its role as a reverse (lipid clearing) cholesterol transporter (4). A highly charged region of SAA1 and 2 (aa 36 ‑ 68) contains putative fibronectin and laminin binding motifs (3). This region also binds heparan sulfate proteoglycans at mildly acidic pH and promotes aggregation of A‑SAA; however, pathogenic amyloid fibrils contain fragments of mouse SAA2, not SAA1 (3, 7, 8). Mouse strains can differ in SAA sequence, expression, and amyloid formation (1, 8 ‑ 10). SAA1 is a ligand for CD36/SR‑B3, SR‑B1, FPRL1, TLR2, and RAGE on monocytes/macrophages, inducing chemotaxis and generation of cytokines and tissue factor (12 ‑ 14). SAA1 can bind the surface of invading gram‑negative bacteria, acting as an opsonin to aid clearance by macrophages (11). SAA1 also binds platelets, probably by engaging fibrinogen on the platelet surface (15).

References
  1. Lowell, C.A. et al. (1986) J. Biol. Chem. 261:8442.
  2. Yamamoto, K-I. and S. Migita (1985) Proc. Natl. Acad. Sci. USA 82:2915.
  3. Uhlar, C.M. and A.S. Whitehead (1999) Eur. J. Biochem. 265:501.
  4. van der Westhuyzen, D.R. et al. (2007) Curr. Opin. Lipidol. 18:147.
  5. Yang, R-Z. et al. (2006) PLoS Med. 3:e287.
  6. Scheja, L. et al. (2008) Exp. Diabetes Res. 2008:230837.
  7. Elimova, E. et al. (2009) FASEB J. 23:3436.
  8. Yu, J. et al. (2000) Lab. Invest. 80:1797.
  9. Thorn, C.F. and A.S. Whitehead (2002) Amyloid 9:229.
  10. deBeer, M.C. et al. (1993) J. Biol. Chem. 268:20606.
  11. Shah, C. et al. (2006) Blood 108:1751.
  12. He, R.L. et al. (2009) Blood 113:429.
  13. Cai, H. et al. (2007) J. Immunol. 178:1852.
  14. Baranova, I.N. et al. (2010) J. Biol. Chem. 285:8492.
  15. Urieli-Shoval, S. et al. (2002) Blood 99:1224.
Entrez Gene IDs
6288 (Human); 20208 (Mouse)
Alternate Names
MGC111216; PIG4; SAA; SAA1; SAA2; serum amyloid A protein; Serum Amyloid A1; TP53I4; tumor protein p53 inducible protein 4

Citations for Recombinant Mouse Serum Amyloid A1 Protein, CF

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

4 Citations: Showing 1 - 4
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  1. An invasive zone in human liver cancer identified by Stereo-seq promotes hepatocyte-tumor cell crosstalk, local immunosuppression and tumor progression
    Authors: Wu, L;Yan, J;Bai, Y;Chen, F;Zou, X;Xu, J;Huang, A;Hou, L;Zhong, Y;Jing, Z;Yu, Q;Zhou, X;Jiang, Z;Wang, C;Cheng, M;Ji, Y;Hou, Y;Luo, R;Li, Q;Wu, L;Cheng, J;Wang, P;Guo, D;Huang, W;Lei, J;Liu, S;Yan, Y;Chen, Y;Liao, S;Li, Y;Sun, H;Yao, N;Zhang, X;Zhang, S;Chen, X;Yu, Y;Li, Y;Liu, F;Wang, Z;Zhou, S;Yang, H;Yang, S;Xu, X;Liu, L;Gao, Q;Tang, Z;Wang, X;Wang, J;Fan, J;Liu, S;Yang, X;Chen, A;Zhou, J;
    Cell research
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  2. Serum Amyloid A1/Toll-Like Receptor-4 Axis, an Important Link between Inflammation and Outcome of TBI Patients
    Authors: V Farré-Alin, A Palomino-A, P Narros-Fer, AB Lopez-Rodr, C Decouty-Pe, A Muñoz-Mont, J Zamorano-F, B Mansilla-F, J Giner-Garc, P García-Fei, M Sáez-Alegr, AJ Palpán-Flo, JM Roda-Frade, CS Carabias, JM Rosa, B Civantos-M, S Yus-Teruel, L Gandía, A Lagares, BJ Hernández-, J Egea
    Biomedicines, 2021-05-25;9(6):.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay
  3. Bacterial Lipoproteins Constitute the TLR2-Stimulating Activity of Serum Amyloid A
    Authors: EJ Burgess, LR Hoyt, MJ Randall, MM Mank, JJ Bivona, PL Eisenhauer, JW Botten, BA Ballif, YW Lam, MJ Wargo, JE Boyson, JL Ather, ME Poynter
    J. Immunol., 2018-08-29;0(0):.
    Species: Human
    Sample Types: Whole Cells
    Applications: Bioassay
  4. High-density lipoprotein inhibits serum amyloid A-mediated reactive-oxygen species generation and NLRP3 inflammasome activation
    Authors: P Shridas, MC De Beer, NR Webb
    J. Biol. Chem., 2018-07-05;0(0):.
    Species: Mouse
    Sample Types: Whole Cells
    Applications: Bioassay

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Recombinant Mouse Serum Amyloid A1 Protein, CF
By Anonymous on 05/23/2020
Application: CellProlif

Recombinant Mouse Serum Amyloid A1 Protein, CF
By Anonymous on 07/25/2018
Application: Immunoassay Standard