Choline Acetyltransferase/ChAT Antibody
Novus Biologicals | Catalog # NBP1-30052
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Key Product Details
Species Reactivity
Validated:
Human, Mouse, Rat, Chicken, Guinea Pig, Primate
Cited:
Mouse, Rat
Applications
Validated:
Immunohistochemistry, Immunohistochemistry-Paraffin, Immunohistochemistry-Frozen, Immunohistochemistry Free-Floating, Immunohistochemistry Whole-Mount, Western Blot, Immunocytochemistry/ Immunofluorescence
Cited:
Immunohistochemistry, Immunohistochemistry-Frozen, Immunohistochemistry Free-Floating, Immunohistochemistry Whole-Mount, Western Blot, Immunocytochemistry/ Immunofluorescence, IF/IHC
Label
Unconjugated
Antibody Source
Polyclonal Goat IgG
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Product Specifications
Immunogen
Native choline acetyltransferase purifed from human placenta
Marker
Cholinergic Neuronal Marker
Specificity
Specific for endogenous levels of the ~70 kDa Choline Acetyltransferase/ChAT protein.
Clonality
Polyclonal
Host
Goat
Isotype
IgG
Theoretical MW
70 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Description
Recommended that the undiluted antibody be aliquoted into smaller working volumes (10-30 uL/vial depending on usage).
Scientific Data Images for Choline Acetyltransferase/ChAT Antibody
Western Blot: Choline Acetyltransferase/ChAT Antibody [NBP1-30052]
Choline Acetyltransferase-ChAT Antibody-Western Blot-NBP1-30052-img0006.jpgImmunocytochemistry/ Immunofluorescence: Choline Acetyltransferase/ChAT Antibody [NBP1-30052]
Choline-Acetyltransferase-ChAT-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-30052-img0005.jpgImmunohistochemistry-Paraffin: Choline Acetyltransferase/ChAT Antibody [NBP1-30052]
Immunohistochemistry-Paraffin: Choline Acetyltransferase/ChAT Antibody [NBP1-30052] - Rat brainstem showing specific labeling using the anti-ChAT antibody. Image courtesy of Dr. Robert Sloviter, University of Arizona.Western Blot: Choline Acetyltransferase/ChAT Antibody [NBP1-30052]
Western Blot: Choline Acetyltransferase/ChAT Antibody [NBP1-30052] - Rat brain lysate showing specific immunolabeling of the ~70k ChAT.Immunocytochemistry/ Immunofluorescence: Choline Acetyltransferase/ChAT Antibody [NBP1-30052]
Choline-Acetyltransferase-ChAT-Antibody-Immunocytochemistry-Immunofluorescence-NBP1-30052-img0004.jpgImmunocytochemistry/ Immunofluorescence: Choline Acetyltransferase/ChAT Antibody [NBP1-30052] -
Immunocytochemistry/ Immunofluorescence: Choline Acetyltransferase/ChAT Antibody [NBP1-30052] - MATR3 loss in alpha -motor neurons & interneurons in the thoracic spinal cord of Matr3S85C/S85C mice. (A) Representative images of 10 & 30 weeks thoracic spinal cord staining for alpha -motor neurons (ChAT+, NeuN+, denoted by white arrows) & gamma -motor neurons (Chat+, NeuN−, denoted by yellow arrows). Scale bar for the spinal cord image denotes 500 μm & the zoomed-in image denotes 50 µm. Quantification of the percentage of motor neurons with reduced MATR3 staining in (B) alpha -motor neurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C) & (C) gamma -motor neurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). Quantification of the number of (D) alpha -motor neurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C) & (E) gamma -motor neurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). (F) Representative images of 10 & 30 weeks PVALB+ interneurons in the thoracic spinal cord. Interneurons with reduced MATR3 staining are denoted by a white asterisk. Scale bar denotes 50 µm. (G) Quantification of the percentage of PVALB+ interneurons with reduced MATR3 staining (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). (H) Quantification of the number of PVALB+ interneurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). Bar graph heights depict mean ± SEM, with each datapoint representing an animal. * p < 0.05, *** p < 0.001, **** p < 0.0001, ns = not significant. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/35205163), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: Choline Acetyltransferase/ChAT Antibody [NBP1-30052] -
Immunocytochemistry/ Immunofluorescence: Choline Acetyltransferase/ChAT Antibody [NBP1-30052] - MATR3 loss in alpha -motor neurons & interneurons in the cervical spinal cord of Matr3S85C/S85C mice. (A) Representative images of 10 & 30 weeks cervical spinal cord staining for alpha -motor neurons (ChAT+, NeuN+, denoted by white arrows) & gamma -motor neurons (ChAT+, NeuN−, denoted by yellow arrows). Scale bar for the spinal cord image denotes 500 μm & the zoomed-in image denotes 50 µm. Quantification of the percentage of motor neurons with reduced MATR3 staining in (B) alpha -motor neurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C) & (C) gamma -motor neurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). Quantification of the number of (D) alpha -motor neurons (10 weeks: n = 6 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C) & (E) gamma -motor neurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). (F) Representative images of 10 & 30 weeks PVALB+ interneurons in the cervical spinal cord. Interneurons with reduced MATR3 staining are denoted by a white asterisk. Scale bar denotes 50 µm. (G) Quantification of the percentage of PVALB+ interneurons with reduced MATR3 staining (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). (H) Quantification of the number of PVALB+ interneurons (10 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C; 30 weeks: n = 3 Matr3+/+, 3 Matr3S85C/S85C). Bar graph heights depict mean ± SEM, with each datapoint representing an animal. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001, ns = not significant. Image collected & cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/35205163), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for Choline Acetyltransferase/ChAT Antibody
Application
Recommended Usage
Immunohistochemistry
1:100
Immunohistochemistry-Paraffin
1:10-1:500
Western Blot
1:100
Application Notes
Use in Immunohistochemistry-Frozen reported in scientific literature (PMID 21912682) Use in Immunohistochemistry-whole mount reported in scientific literature (PMID 24630395). ICC/IF reported in scientific literature (PMID 23095258). Use in Immunohistochemistry-free floating reported in scientific literature (PMID: 30261285).
Formulation, Preparation, and Storage
Purification
Affinity purified
Formulation
PBS and 5 mg/ml BSA
Preservative
0.2% Sodium Azide
Concentration
Please see the vial label for concentration. If unlisted please contact technical services.
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at -20C. Avoid freeze-thaw cycles.
Background: Choline Acetyltransferase/ChAT
Additional Choline Acetyltransferase/ChAT Products
Product Documents for Choline Acetyltransferase/ChAT Antibody
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for Choline Acetyltransferase/ChAT Antibody
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for Choline Acetyltransferase/ChAT Antibody
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
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