Tetrahydroisoquinolines (TIQs) are structurally similar to MPTP, an agent known to cause Parkinsonism. TIQs may play a role in pathogenesis of Parkinson's Disease.
Key Product Details
Species Reactivity
Multi-Species
Applications
Immunohistochemistry
Label
Unconjugated
Antibody Source
Monoclonal Mouse IgG2B Clone # 106814
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Product Specifications
Immunogen
Carrier protein-coupled N‑Me‑6,7-diOH-TIQ
Specificity
Recognizes N‑Me‑6,7‑diOH‑TIQ in immunoassays. The specificity was determined by a competition type assay where the N‑Me‑6,7‑diOH‑TIQ labeled with biotin at position 5 or 8 competed with another compound for binding to the antibody binding site. The detection limit of biotinylated N‑Me‑6,7‑diOH‑TIQ in assays where the molecule was captured by the antibody coated on microplates and developed by HRP‑streptavidin was 5 nM. The dissociation constants of the interaction between the antibody and N‑Me‑6,7‑diOH‑TIQ and its biotinylated analog were 0.2 and 0.5 µM, respectively. This antibody specifically recognizes N‑Me‑6,7‑diOH‑TIQ and shows 60% cross‑reactivity with 6,7‑diOH‑TIQ, 15% cross‑reactivity with 1,N‑di‑Me‑6,7‑diOH‑TIQ, 3% cross‑reactivity with 1‑Me‑6,7‑diOH‑TIQ, and less than 1% or no cross‑reactivity with tetrahydroisoquinoline (TIQ), 5‑OH‑isoquiniline, 5‑OH‑N‑Me‑isoquinolinium, tetrahydropapaveroline, 9H‑pyrido[3,4‑b]indole, and 1,2,3,4‑tetrahydro‑9H‑pyrido[3,4‑b]indole. The percent cross‑reactivity is expressed by the relative value, which produced 50% inhibition of interaction between the biotin‑labeled N‑methyl‑6,7‑dihydroxytetrahydroisoquinoline and the other compound.
Clonality
Monoclonal
Host
Mouse
Isotype
IgG2B
Applications for N‑Me‑6,7‑diOH‑TIQ Antibody
Application
Recommended Usage
Immunohistochemistry
8-25 µg/mL
Sample: Immersion fixed paraffin-embedded sections of human Alzheimer's disease brain
Sample: Immersion fixed paraffin-embedded sections of human Alzheimer's disease brain
Formulation, Preparation, and Storage
Purification
Protein A or G purified from ascites
Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
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Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.
Shipping
Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.
Stability & Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: N-Me-6,7-diOH-TIQ
Alternate Names
7diOHTIQ, NMe6
Additional N-Me-6,7-diOH-TIQ Products
Product Documents for N‑Me‑6,7‑diOH‑TIQ Antibody
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Product Specific Notices for N‑Me‑6,7‑diOH‑TIQ Antibody
For research use only
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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
- IHC Sample Preparation (Frozen sections vs Paraffin)
- 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 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 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
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
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