SAA Antikörper

Produktnummer ABIN2191977

Produktdetails anti-SAA Antikörper

Target: SAA (Serum Amyloid A (SAA))

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser SAA Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunoassay (IA), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Sterilität: 0.2 μm filtered

Klon: Reu86-5

Anwendungsinformationen

Applikationshinweise: For western blotting, immunohistology dilutions to be used depend on detection system applied. It is recommended that users test the reagent and determine their own optimal dilutions. The typical starting working dilution is 1:10.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: PBS, containing 0.02 % sodium azide and 0.1 % bovine serum albumin.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C

Informationen zur Lagerung: Product should be stored at 4 °C. Under recommended storage conditions, product is stable for one year.

Haltbarkeit: 12 months

Referenzen für anti-SAA Antikörper (ABIN2191977)

Hazenberg, Limburg, Bijzet, van Rijswijk: "A quantitative method for detecting deposits of amyloid A protein in aspirated fat tissue of patients with arthritis." in: Annals of the rheumatic diseases, Vol. 58, Issue 2, pp. 96-102, (1999) (PubMed).

Wilkins, Gallimore, Tennent, Hawkins, Limburg, van Rijswijk, Moore, Pepys: "Rapid automated enzyme immunoassay of serum amyloid A." in: Clinical chemistry, Vol. 40, Issue 7 Pt 1, pp. 1284-90, (1994) (PubMed).

Details zu SAA

Target: SAA (Serum Amyloid A (SAA))

Andere Bezeichnung: Serum Amyloid A (SAA Produkte)

Synonyme: PIG4 antikoerper, SAA antikoerper, SAA2 antikoerper, TP53I4 antikoerper, zgc:103580 antikoerper, saa antikoerper, SAA1 antikoerper, Saa-1 antikoerper, Saa2 antikoerper, serum amyloid A1 antikoerper, serum amyloid A antikoerper, serum amyloid A protein antikoerper, serum amyloid A-3 antikoerper, HPS5, biogenesis of lysosomal organelles complex 2 subunit 2 antikoerper, serum amyloid A2 antikoerper, serum amyloid A 1 antikoerper, SAA1 antikoerper, saa antikoerper, LOC476879 antikoerper, SAA antikoerper, SAA3 antikoerper, HPS5 antikoerper, SAA2 antikoerper, Saa1 antikoerper, LOC100270725 antikoerper

Hintergrund: The serum amyloid A (SAA) family comprises a number of differentially expressed apolipoproteins, acute- phase SAA1 and SAA2, the former being the major component in plasma, and constitutive SAAs (C- SAAs). Although the liver is the primary site of synthesis of both SAA types extrahepatic production has been reported. The in vivo concentrations increase by as much as 1000-fold during inflammation. Several studies have stressed its importance in the diagnosis and monitoring of various diseases. Pathological SAA values are often detected in association with normal CRP concentrations, SAA rises earlier and more sharply than CRP. Recently, a broader view of SAA expression and function has been emerging. Expression studies show production of SAA proteins in histologically normal, atherosclerotic, Alzheimer, inflammatory, and tumor tissues. SAA has been found to have binding sites for high density lipoproteins, calcium, laminin, and heparin/heparan-sulfate. Also adhesion motifs were identified and new functions, affecting cell adhesion, migration, proliferation and aggregation discovered. These findings emphasize the importance of SAA in various physiological and pathological processes, including inflammation, atherosclerosis, thrombosis, AA- amyloidosis, rheumatoid arthritis, and neoplasia. SAA has also a number of immunomodulatory roles, it can induce chemotaxis and adhesion molecule expression, has cytokine-like properties and can promote the upregulation of metalloproteinases. It enhances the binding of high-density lipoprotein to macrophages and thus helps in the delivery of lipids to sites of injury for use in tissue repair. It is thus thought to be an integral part of the disease processes. In addition, recent experiments suggest that SAA may play a "housekeeping" role in normal human tissues. Elevated levels of SAA over time predispose to secondary amyloidosis, extracellular accumulation of amyloid fibrils, derived from a circulating precursor, in various tissue and organs. The most common form of amyloidosis occurs secondary to chronic inflammatory disease, particularly rheumatoid arthritis. The antibody is raised against human SAA and Helix Pomatia Haemocyanine. It reacts with SAA-1 type.