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

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Antigen
Epitope
Chain mu
557
373
291
63
56
47
43
28
6
6
2
1
1
1
1
Reactivity
Mouse (Murine)
1175
551
230
88
79
66
65
57
56
55
53
39
35
21
19
15
15
7
5
5
2
1
1
Host
Goat
1243
646
504
143
38
11
9
9
4
3
3
1
Clonality
Polyclonal
Conjugate
Texas Red (TR)
351
342
270
156
98
74
65
53
25
25
23
22
22
19
18
16
16
16
16
15
14
14
13
12
9
7
7
5
5
5
4
4
4
4
4
3
3
3
3
2
2
2
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, 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).