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Goat anti-Mouse (Murine) IgG (Heavy & Light Chain) Antibody (Texas Red (TR))

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Antigen
Epitope: Heavy & Light Chain
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Reactivity: Mouse (Murine)
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Host: Goat
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Clonality: Polyclonal
Conjugate: Texas Red (TR)
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Application: Immunoassay (IA)
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Catalog No. ABIN101770

$229.00
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Shipping to: United States ( Change Change )
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Quantity

Price

1 mg

$229.00

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Immunogen	Mouse IgG whole molecule
Isotype	IgG
Specificity	IgG (H&L)
Characteristics	Mouse IgG (H&L) Antibody Texas Red™ Conjugated Pre-Adsorbed antibodies are designed for immunofluorescence microscopy, fluorescence based plate assays (FLISA) and fluorescent western blotting. This product is also suitable for multiplex analysis, including multicolor imaging, utilizing various commercial platforms. Concentration Definition: by UV absorbance at 280 nm

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Research Area	Immunology, Secondary Antibodies

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Application Notes	Optimal working dilutions should be determined experimentally by the investigator.
Comment	Texas Red™ is a registered trademark of Molecular Probes Inc.
Restrictions	For Research Use only

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Format	Lyophilized
Reconstitution	Restore with deionized water (or equivalent)
Concentration	1.0 mg/mL
Buffer	0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Preservative	Sodium azide
Precaution of Use	WARNING: Reagents contain sodium azide. Sodium azide is very toxic if ingested or inhaled. Avoid contact with skin, eyes, or clothing. Wear eye or face protection when handling. If skin or eye contact occurs, wash with copious amounts of water. If ingested or inhaled, contact a physician immediately. Sodium azide yields toxic hydrazoic acid under acidic conditions. Dilute azide-containing compounds in running water before discarding to avoid accumulation of potentially explosive deposits in lead or copper plumbing.
Handling Advice	Product is photosensitive and should be protected from light.

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Background publications	Titus, Haugland, Sharrow, Segal: "Texas Red, a hydrophilic, red-emitting fluorophore for use with fluorescein in dual parameter flow microfluorometric and fluorescence microscopic studies." in: Journal of immunological methods, Vol. 50, Issue 2, pp. 193-204, 1982 (PubMed).