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Description
Research Area
Images & Validation
−| Tested Applications | FC, IF, IHC-P, WB |
|---|---|
| Dilution Range | IF: 1:25, WB: 1:1000, IHC-P: 1:25, IHC-P: 1:25, FC: 1:25 |
| Reactivity | Human, Mouse |
Key Properties
−| Antibody Type | Primary Antibody |
|---|---|
| Host | Mouse |
| Clonality | Monoclonal |
| Isotype | IgG1,κ |
| Immunogen | This antibody is generated from a mouse immunized with a recombinant protein. |
| Target | CHRM2 |
| Molecular Weight | 51715 Da |
| Conjugation | Unconjugated |
Storage & Handling
−| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles |
|---|---|
| Form/Appearance | Purified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, followed by dialysis against PBS. |
| Expiration Date | 12 months from date of receipt. |
| Disclaimer | For research use only |
Alternative Names
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ELISA, IF, WB
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Polyclonal
Unconjugated
100 μl, 50 μlMouse Cholinergic Receptor, Muscarinic 2 (CHRM2) ELISA Kit [orb777788]
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0.16-10 ng/mL
0.052 ng/mL
48 T, 96 TRat Cholinergic Receptor, Muscarinic 2 (CHRM2) ELISA Kit [orb780439]
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0.16-10 ng/mL
0.053 ng/mL
96 T, 48 THuman Cholinergic Receptor, Muscarinic 2 (CHRM2) ELISA Kit [orb775671]
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0.16-10 ng/mL
0.056 ng/mL
96 T, 48 T

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Immunohistochemical analysis of paraffin-embedded H. heart section using CHRM2. Diluted at 1:25 dilution. A undiluted biotinylated goat polyvalent antibody was used as the secondary, followed by DAB staining.

Immunohistochemical analysis of paraffin-embedded H. brain section using CHRM2. Diluted at 1:25 dilution. A undiluted biotinylated goat polyvalent antibody was used as the secondary, followed by DAB staining.

Fluorescent image of SH-SY5Y cells stained with CHRM2 Antibody. Diluted at 1:25 dilution. An Alexa Fluor 488-conjugated goat anti-mouse lgG at 1:400 dilution was used as the secondary antibody (green). DAPI was used to stain the cell nuclear (blue).

All lanes: Anti-CHRM2 Antibody at 1:1000 dilution. Lane 1: human brain lysates. Lane 2: SH-SY5Y whole cell lysates. Lane 3: U-87 MG whole cell lysates. Lane 4: Y79 whole cell lysates. Lane 5: Neuro-2a whole cell lysates. Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Mouse IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size: 52 kDa. Blocking/Dilution buffer: 5% NFDM/TBST.

Overlay histogram showing SH-SY5Y cells stained with (green line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 90% methanol for 10 min. The cells were then icubated in 2% bovine serum albumin to block non-specific protein-protein interactions followed by the antibody (, 1:25 dilution) for 60 min at 37°C. The secondary antibody used was Alexa Fluor 488 goat anti-mouse lgG (166821) at 1/200 dilution for 40 min at 37°C. Isotype control antibody (blue line) was mouse IgG1 (1 μg/1x10^6 cells) used under the same conditions. Acquisition of >10000 events was performed.
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CHRM2 Antibody (orb1788044)
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