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Goat anti-Mouse (Murine) IgM (Chain mu) Antibody (Texas Red (TR))

Details for Product No. ABIN102679, Supplier: Log in to see
Antigen
Epitope
Chain mu
584
260
223
60
44
17
16
6
4
4
1
1
1
Reactivity
Mouse (Murine)
905
464
213
84
77
66
66
60
50
44
43
29
29
19
15
14
5
4
2
1
1
1
Host
Goat
1124
467
400
121
32
11
9
9
2
1
Clonality
Polyclonal
Conjugate
Texas Red (TR)
310
294
236
131
78
74
53
42
26
16
13
11
11
11
11
10
10
9
7
7
5
4
4
4
4
4
3
3
3
2
2
2
2
2
2
2
2
2
2
1
1
1
1
1
1
1
1
1
1
1
1
Application
FLISA, Immunomicroscopy (IM), Western Blotting (WB)
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Immunogen Mouse IgM mu heavy chain
Isotype IgG
Specificity IgM µ chain
Characteristics Concentration Definition: by UV absorbance at 280 nm
Research Area Secondary Antibodies
Application Notes This product is 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.
Comment

Texas Red™ is a registered trademark of Molecular Probes Inc.

Restrictions For Research Use only
Format Lyophilized
Reconstitution Restore with deionized water (or equivalent)
Concentration 2.0 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.
Background publications Titus, Haugland, Sharrow et al.: "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).