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Die folgenden MAPmates™ sollten nicht zusammen analysiert werden: -MAPmates™, die einen unterschiedlichen Assaypuffer erfordern. -Phosphospezifische und MAPmate™ Gesamtkombinationen wie Gesamt-GSK3β und Gesamt-GSK3β (Ser 9). -PanTyr und locusspezifische MAPmates™, z.B. Phospho-EGF-Rezeptor und Phospho-STAT1 (Tyr701). -Mehr als 1 Phospho-MAPmate™ für ein einziges Target (Akt, STAT3). -GAPDH und β-Tubulin können nicht mit Kits oder MAPmates™, die panTyr enthalten, analysiert werden.
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Gewähltes Kit
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96-Well Plate
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48-602MAG
Buffer Detection Kit for Magnetic Beads
1 Kit
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Recognizes the ~120 kDa muscarinic M1 acetylcholine receptor protein in rat brain. Supplied with a control peptide.
Catalogue Number
475923
Brand Family
Calbiochem®
Synonyms
Anti-M1
Application Data
Detection of rat muscarinic M1 acetylcholine receptor by immunoblotting. Samples: Extract from rat brain membranes left untreated (lane 1) and treated by preincubation with the fusion protein antigen (lane 2). Primary antibody: Anti-Muscarinic M1 Acetylcholine Receptor (227-353) Rabbit pAb (Cat. No. 475923) (1:200). Detection: chemiluminescence.
References
References
Levey, A.I., et al. 1991. J. Neurosci.11, 3218. Levey, A.I., et al. 1990. FEBS Lett.275, 65. Smith. D.B., et al. 1988. Gene 67, 31. Allard, W.J., et al. 1987. Nucleic Acids Res.15, 10604. Peralta, E.G., et al. 1987. EMBO J.6, 3923.
Product Information
Form
Lyophilized
Formulation
50 µl antibody lyophilized from PBS, 1% BSA, pH 7.4 and 60 µg lyophilized control protein.
Positive control
M1-GST fusion protein (supplied) or rat brain
Preservative
≤0.1% sodium azide (antibody only)
Applications
Application References
Immunohistochemistry, Immunoprecipitation
Levey, A.I., et al. 1991. J. Neurosci.11, 3218.
Immunoprecipitation
Levey, A.I., et al. 1990. FEBS Lett.275, 65.
Immunoblotting (1:200-1:300, chemiluminescence) Immunohistochemistry (see application references) Immunoprecipitation (see application references)
Application Comments
The epitope is specific for M1 and is not similar to any other known protein. To reduce non-specific staining, centrifuge all antibody preparations before use (10000 x g for 5 min) to remove any aggregates. For use as a positive control in immunoblotting, use 10 ng/lane of the M1-GST fusion protein (minigel). For use as a negative control, preincubate 3-5 µg of M1-GST fusion protein with 1 µg antibody for 1 h at room temperature. Variables associated with assay conditions will dictate the optimal working dilution.
Biological Information
Immunogen
a recombinant protein consisting of amino acids 227-353 of the i3 intracellular loop of human M1 muscarinic acetylcholine receptor fused to GST
Immunogen
Human
Host
Rabbit
Isotype
IgG
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code
Ambient Temperature Only
Toxicity
Standard Handling
Storage
-20°C
Do not freeze
Ok to freeze
Special Instructions
Reconstitute the antibody with 50 µl dH₂O to yield a stock concentration of 300 µg/ml. For long-term storage, aliquot the antibody and freeze (-20°); for short-term storage, refrigerate (4°C). Further dilutions should be made in a physiological buffer containing a carrier protein such as 1-3% BSA. Reconstitute the M1-GST fusion protein with 100 µl H₂O, aliquot, and freeze (-20°C). Avoid freeze/thaw cycles of solutions.
Levey, A.I., et al. 1991. J. Neurosci.11, 3218. Levey, A.I., et al. 1990. FEBS Lett.275, 65. Smith. D.B., et al. 1988. Gene 67, 31. Allard, W.J., et al. 1987. Nucleic Acids Res.15, 10604. Peralta, E.G., et al. 1987. EMBO J.6, 3923.
Datenblatt
Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.
Revision
07-August-2007 RFH
Synonyms
Anti-M1
Application
Immunoblotting (1:200-1:300, chemiluminescence) Immunohistochemistry (see application references) Immunoprecipitation (see application references)
Application Data
Detection of rat muscarinic M1 acetylcholine receptor by immunoblotting. Samples: Extract from rat brain membranes left untreated (lane 1) and treated by preincubation with the fusion protein antigen (lane 2). Primary antibody: Anti-Muscarinic M1 Acetylcholine Receptor (227-353) Rabbit pAb (Cat. No. 475923) (1:200). Detection: chemiluminescence.
Description
Rabbit polyclonal antibody adsorbed against immobilized non-relevant GST fusion protein followed by immunoaffinity chromatography. Recognizes the ~120 kDa muscarinic M1 acetylcholine receptor protein. Supplied with a control protein consisting of recombinant M1-GST fusion protein.
Host
Rabbit
Immunogen species
Human
Immunogen
a recombinant protein consisting of amino acids 227-353 of the i3 intracellular loop of human M1 muscarinic acetylcholine receptor fused to GST
Isotype
IgG
Species
human, rat
Positive control
M1-GST fusion protein (supplied) or rat brain
Form
Lyophilized
Formulation
50 µl antibody lyophilized from PBS, 1% BSA, pH 7.4 and 60 µg lyophilized control protein.
Preservative
≤0.1% sodium azide (antibody only)
Comments
The epitope is specific for M1 and is not similar to any other known protein. To reduce non-specific staining, centrifuge all antibody preparations before use (10000 x g for 5 min) to remove any aggregates. For use as a positive control in immunoblotting, use 10 ng/lane of the M1-GST fusion protein (minigel). For use as a negative control, preincubate 3-5 µg of M1-GST fusion protein with 1 µg antibody for 1 h at room temperature. Variables associated with assay conditions will dictate the optimal working dilution.
Storage
-20°C
Do Not Freeze
Ok to freeze
Special Instructions
Reconstitute the antibody with 50 µl dH₂O to yield a stock concentration of 300 µg/ml. For long-term storage, aliquot the antibody and freeze (-20°); for short-term storage, refrigerate (4°C). Further dilutions should be made in a physiological buffer containing a carrier protein such as 1-3% BSA. Reconstitute the M1-GST fusion protein with 100 µl H₂O, aliquot, and freeze (-20°C). Avoid freeze/thaw cycles of solutions.
Toxicity
Standard Handling
References
Levey, A.I., et al. 1991. J. Neurosci.11, 3218. Levey, A.I., et al. 1990. FEBS Lett.275, 65. Smith. D.B., et al. 1988. Gene 67, 31. Allard, W.J., et al. 1987. Nucleic Acids Res.15, 10604. Peralta, E.G., et al. 1987. EMBO J.6, 3923.
Application references
Immunohistochemistry, Immunoprecipitation
Levey, A.I., et al. 1991. J. Neurosci.11, 3218.
Immunoprecipitation
Levey, A.I., et al. 1990. FEBS Lett.275, 65.