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SAA1 (show SAA1 ELISA Kits)/2 produced by macrophages promotes early lesion formation in the ascending aorta in LDLR (show LDLR ELISA Kits) knockout mice.
CE/J mice possess functional Saa1 (show SAA1 ELISA Kits) and Saa2 (show SAA1 ELISA Kits) genes with identical amino acid sequence.
Its gene hold broader diversity and greater complexity and these characteristics were likely attained through gene duplication and repeated gene conversion events in the Mus (show TRPV6 ELISA Kits) lineage.
The absence of endogenous SAA1.1 and 2.1 does not affect atherosclerotic lipid deposition in apolipoprotein E (show APOE ELISA Kits)-deficient mice fed either normal or Western diets.
High level SAA (show SAA1 ELISA Kits) expression induced amyloidosis in all mice after a short, slightly variable delay.
Pathogenic serum amyloid A 1.1 shows a long oligomer-rich fibrillation lag (show STMN1 ELISA Kits) phase contrary to the highly amyloidogenic non-pathogenic SAA2.2
These results suggest that the carboxy terminus of SAA (show SAA1 ELISA Kits), which is highly conserved among SAA (show SAA1 ELISA Kits) sequences in all vertebrates, might play important structural roles, including modulating the folding, oligomerization, misfolding, and fibrillation of SAA (show SAA1 ELISA Kits).(Saa2 (show SAA1 ELISA Kits))
The ability of SAA2.2 to form different oligomeric species in vitro along with its marginal stability, suggest that the structure of SAA (show SAA1 ELISA Kits) might be modulated in vivo to form different biologically relevant species.
SAA (show SAA1 ELISA Kits) does not impact High Density Lipoprotein levels, apoA-I (show APOA1 ELISA Kits) clearance, or High Density Lipoprotein size
Many functional and pathological roles attributed to serum amyloid A may rely on its precarious structure, modulated by its interaction with ligands under homeostasis conditions and during the acute phase response.
The prevalence of the SAA2 (show SAA1 ELISA Kits) polymorphisms (rs 2445174 and rs2468844) did not differ significantly between the groups of ankylosing spondylitis patients with and without amyloidosis.
successful quantification of SAA2 (show SAA1 ELISA Kits) in crude serum by MRM, for the first time, shows that SAA2 (show SAA1 ELISA Kits) can be a good biomarker for the detection of lung cancers.
Data show that both rs12218 of the SAA1 gene and rs2468844 of SAA2 gene are associated with carotid IMT in healthy Han Chinese subjects.
The glucocorticoid response element of the SAA2 (show SAA1 ELISA Kits) promoter is dysfunctional compared to that of SAA1 (show SAA1 ELISA Kits), hence glucocorticoids are unable to enhance the cytokine-driven transcriptional activity of SAA2 (show SAA1 ELISA Kits).
saa2 (show SAA1 ELISA Kits) is regulated by tumor necrosis factor-alpha (show TNF ELISA Kits), interleukin-6 (show IL6 ELISA Kits), and glucocorticoids in hepatic and epithelial cells.
SAA1a/a genotype is one genetic factor that confers a significant risk for amyloidosis in the Turkish FMF (show MEFV ELISA Kits) population but neither SAA1 (show SAA1 ELISA Kits) nor SAA2 (show SAA1 ELISA Kits) genotypes had a significant effect on SAA (show SAA1 ELISA Kits) level.
Increased expression of SAA2 (show SAA1 ELISA Kits) by adipocytes in obesity may play a critical role in local and systemic inflammation and free fatty acid production and could be a direct link between obesity and its comorbidities.
CRP (show CRP ELISA Kits) and SAA (show SAA1 ELISA Kits) strongly correlated up to the fifth day of observation but were not good predictors of mortality in septic shock.
Major acute phase reactant. Apolipoprotein of the HDL complex.
serum amyloid A2
, serum amyloid A 1
, serum amyloid A-2 protein
, serum amyloid A protein