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MABF291

Sigma-Aldrich

Anti-S100A8/S100A9 Antibody, clone 5.5

clone 5.5, from mouse

Synonym(e):

Protein S100-A9, Calgranulin-B, Calprotectin L1H subunit, Leukocyte L1 complex heavy chain, Migration inhibitory factor-related protein 14, S100 calcium-binding protein A9, AMRP-14, p14, Protein S100-A8, Calgranulin-A, Calprotectin L1L subunit, Cystic fi

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About This Item

UNSPSC-Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Biologische Quelle

mouse

Qualitätsniveau

Antikörperform

purified immunoglobulin

Antikörper-Produkttyp

primary antibodies

Klon

5.5, monoclonal

Speziesreaktivität

human

Methode(n)

ELISA: suitable
flow cytometry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

Isotyp

IgG1κ

NCBI-Hinterlegungsnummer

UniProt-Hinterlegungsnummer

Versandbedingung

wet ice

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

Allgemeine Beschreibung

S100A8, also known as Protein S100-A8, Calgranulin-A, Calprotectin L1L subunit, Cystic fibrosis antigen (CFAG), Leukocyte L1 complex light chain, Migration inhibitory factor related protein 8 (MRP-8), p8, S100 calcium binding protein A8, or Urinary stone protein band A, and encoded by the gene S100A8/CAGA/CFAG/MRP8, is an important protein that binds both zinc and calcium and plays an important role in the regulation of inflammatory processes and immune response. Found in complex with its partner S100A9, S100A8 facilitates chemotaxis, fatty acid trafficking, cytoskeleton reorganization, and NAPDPH oxidase activation and other intracellular activities, as well as a host of extracellular induced activities such as extracellular proinflammatory, antimicrobial, oxidant scavenging, and apoptotic activities . Additionally S100A8 can act as a potent autoimmunity amplifier and appears to augment various cancers and their spread when over expressed. S100A8 is widely expressed and used as biomarker in patients with inflammatory diseases and as a cancer marker in multiple forms of cancer.

Spezifität

This antibody detects both S100A8 and S100A9.

Immunogen

Whole cells expressing Human S100A8 & S100A9.

Anwendung

Research Category
Entzündung & Immunologie
Research Sub Category
Immunologische Signalübertragung
This Anti-S100A8/S100A9 Antibody, clone 5.5 is validated for use in Flow Cytometry and Immunoprecipitation and Immunohistochemistry and ELISA and Western Blotting for the detection of S100A8/S100A9.
Western Blotting Analysis: A representative lot of this antibody was used to detect S100A8/S100A9 in Human monocyte and neutrophil extracts (Edgeworth, J., et al., (1991) JBC. 266(12):7706-7713).
Western Blotting Analysis: A representative lot of this antibody was used to detect S100A8/S100A9 in neutrophil extracts (Hogg et al., 1989).
Immunoprecipitation Analysis: A representative lot of this antibody was used to detect S100A8/S100A9 in Human monocyte and neutrophil lysate (Edgeworth, J., et al., (1991) JBC. 266(12):7706-7713).
Immunoprecipitation Analysis: A representative lot of this antibody was used to detect S100A8/S100A9 in MRP-8 and TL-14 mutant lysate (Hessian P.A., et al., (2001) Eur. J. Biochem. 268:353-363).
Immunohistochemistry Analysis: A representative lot of this antibody was used to detect S100A8/S100A9 in Human Bronchus tissue (Hogg, N., et al., (1989) Eur. J. Immunol. 19:1053-1061).
Immunohistochemistry Analysis: A representative lot of this antibody was used to detect S100A8/S100A9 in spleen and thymus tissue (Hogg, N., et al., (1989) Eur. J. Immunol. 19:1053-1061).
ELISA: A representative lot of this antibody was used to detect S100A8/S100A9 in ELISA (Ryckman, C., et al., (2003) Arthritis & Rheumatism. 48(8):2310-2320).

Qualität

Evaluated by Flow Cytometry on Human PBMCs.

Flow Cytometry Analysis: A 1:80 dilution (0.25 µg) of this antibody detected S100A8 and/or S100A9 in 1x10E6 PBMCs.

Zielbeschreibung

~8 kda(11kDa) and 14 kDa and as a heterodimer it would be ~24 kDa (under native conditions)

Physikalische Form

Protein G Purified
Format: Purified
Purified mouse monoclonal IgG1κ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Lagerung und Haltbarkeit

Stable for 1 year at 2-8°C from date of receipt.

Sonstige Hinweise

Concentration: Please refer to lot specific datasheet.

Haftungsausschluss

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.

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Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Identification of p8,14 as a highly abundant heterodimeric calcium binding protein complex of myeloid cells.
Edgeworth, J, et al.
The Journal of Biological Chemistry, 266, 7706-7713 (1991)
Monoclonal antibody 5.5 reacts with p8,14, a myeloid molecule associated with some vascular endothelium.
Hogg, N, et al.
European Journal of Immunology, 19, 1053-1061 (1989)
P A Hessian et al.
European journal of biochemistry, 268(2), 353-363 (2001-02-13)
The S100 calcium-binding proteins MRP-8 (S100A8) and MRP-14 (S100A9) form a heterodimeric complex in the cytosol of monocyte and neutrophil cell types circulating in peripheral blood. This complex, but not the individual subunit proteins, is specifically recognized by mAb 27E10.
Carle Ryckman et al.
Arthritis and rheumatism, 48(8), 2310-2320 (2003-08-09)
To examine the role of chemokines, S100A8, and S100A9 in neutrophil accumulation induced by the causative agent of gout, monosodium urate monohydrate (MSU) crystals. MSU crystal-induced neutrophil migration was studied in the murine air-pouch model. Release of chemokines, S100A8, S100A9

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