CNPase Antibody - BSA Free
Novus Biologicals | Catalog # NB100-1935
Key Product Details
Species Reactivity
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Label
Antibody Source
Format
Product Specifications
Immunogen
Localization
Marker
Clonality
Host
Isotype
Theoretical MW
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.
Scientific Data Images for CNPase Antibody - BSA Free
Immunohistochemistry: CNPase Antibody [NB100-1935]
Immunohistochemistry: CNPase Antibody [NB100-1935] - A tissue section through an adult mouse brain showing CNPase (brown staining) in white matter tracts and the granule cell layer of the cerebellum.Applications for CNPase Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry
Western Blot
Formulation, Preparation, and Storage
Purification
Formulation
Format
Preservative
Concentration
Shipping
Stability & Storage
Background: CNPase
Alternate Names
Entrez Gene IDs
Gene Symbol
UniProt
Additional CNPase Products
Product Documents for CNPase Antibody - BSA Free
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 CNPase Antibody - BSA Free
Chicken products cannot be exported to Canada.
Purification Notes
After repeated injections, immune eggs were collected, the IgY fractions were purified from the yolks, and then affinity-purified using a peptide column. The concentrations of the eluates were then adjusted to 100 ug/ml, and the preparation was filter-sterilized.
Storage Notes
Store at 4C in the dark. Under these conditions, the antibodies should have a shelf life of at least 12 months (provided they remain sterile). Do not freeze these antibodies unless you want to store them for longer periods of time. Note, however, that each time an antibody preparation is frozen, about half of its binding activity is lost.
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 CNPase Antibody - BSA Free
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Protocols
View specific protocols for CNPase Antibody - BSA Free (NB100-1935):
Citrate Buffer Antigen Retrieval Protocol
Background: Formaldehyde fixation (2% or 4%, or as a component of 10% formalin) produces protein cross-links in tissues that tends to interfere with antibody penetration. This seems to be particularly true of paraffin- embedded formaldehyde-fixed tissue. Since chicken IgY antibodies are larger than rabbit or mouse IgG's, "extra steps" may be necessary to compensate for their larger size.
The citrate-based "antigen retrieval" protocol outlined below has been shown to improve chicken IgY antibody penetration into 4% formalde- hyde-fixed paraffin-embedded sections, and can increase the degree and intensity of immunoreactivity and immunostaining.
Reagents (NOTE: You can use either the Sodium Citrate or Citric Acid Buffers in step #3, below)
"Sodium Citrate Buffer" (10mM Sodium Citrate, 0.05% Tween 20, pH 6.0)
Weigh out 2.94 grams of trisodium citrate (dihydrate). Dissolve in approximately
900 mls of deionized, distilled water. Adjust the pH to 6.00 with 1.0 N HCl. Add
0.5 ml of Tween-20. Mix. Bring up the volume to 1.0 litres with water. Store this solution at room temperature for 3 months or at 4C for longer periods.
"Citric Acid Buffer" (10mM Citric Acid, 0.05% Tween 20, pH 6.0)
Weigh out 1.92 grams of citric acid (anhydrous). Dissolve in approximately 900 mls of deionized, distilled water. Adjust the pH to 6.0 with 1.0 N NaOH. Add
0.5 ml of Tween-20. Mix. Bring up the volume to 1.0 litres with water. Store this solution at room temperature for 3 months or at 4C for longer periods.
"Phosphate-Buffered Saline" [PBS, 10 mM Sodium phosphate-buffered (pH
7.2) isotonic (0.9%, w/v) saline solution] PBS Tween (0.05% Tween 20 in PBS)
Ethanol (80%, 90%, 95%, 100%) diluted with water
Xylene
Procedure (for use with paraffin-embedded sections):
1 Deparaffinize tissue sections in 2 changes of xylene (5 minutes each).
2. Hydrate in 2 changes of 100% ethanol (3 minutes each), 95% ethanol (1 minute),
90% ethanol (1 minute), 80% ethanol (1 minute). Rinse in distilled water.
3. Pre-heat steamer or water bath with staining dish containing either Sodium
Citrate Buffer or Citrate Buffer. Wait until temperature reaches 95-100 degrees C.
NOTE: Microwave or pressure cooker can be used as an alternative as a heating source.
4. Immerse slides in the staining dish. Place the lid loosely on the staining dish and incubate for 20-40 minutes (optimal incubation times will vary).
5. Remove the staining dish, and allow it to cool to room temperature (for 20 minutes or so).
6. Rinse sections in PBS Tween twice for 2 minutes each time.
NOTE: The remainder of this protocol is meant to be a suggestion, and can be substituted with your regular immunostaining protocol.
7. Block sections for 30 minutes with Blocking buffer diluted 1:10 with water.
8. Incubate sections with primary antibody at appropriate dilution in antibody dilution buffer overnight at 4 degrees C. Since chicken IgY antibodies are larger than mammalian IgG's, this overnight incubation allows more time for antibody penetration into tissue sections.
9. Rinse sections with PBS Tween 20 twice for 5 minutes each time.
10. Incubate sections with labeled secondary antibody (see NOTE, below) at appropriate dilution (for one hour at room temperature) in a 1:100 dilution of blocking buffer (diluted in PBS).
11. Rinse with PBS Tween 20 for three times for 5 minutes each time.
NOTE: This protocol may use HRP- or fluorescently-labeled secondary antibodies produced in goats or rabbits.
References:
1. Shi SR, Chaiwun B, Young L, Cote RJ, Taylor CR. (1993). Antigen retrieval technique utilizing citrate buffer or urea solution for immunohistochemical demonstration of androgen receptor in formalin-fixed paraffin sections. J Histochem Cytochem 41 (11): 1599-1604.
2. Kanai K, Nunoya T, Shibuya K, Nakamura T, Tajima M (1998). Variations in effectiveness of antigen retrieval pretreatments for diagnostic immunohistochemistry. Res Vet Sci 64 (1): 57-
61.
3. Brown RW, Chirala R. (1995). Utility of microwave-citrate antigen retrieval in diagnostic immunohistochemistry. Mod Pathol 8 (5): 515-20.
4. Morgan JM, Navabi H, Schmid KW, Jasani B (1994). Possible role of tissue-bound calcium ions in citrate-mediated high-temperature antigen retrieval. J Pathol 174 (4): 301-7.
5. Pellicer EM, Sundblad A (1994). Antigen retrieval by microwave oven with buffer of citric acid.
Medicina (B Aires). 54 (2): 129-32.
6. Shi SR, Chaiwun B, Young L, Cote RJ, Taylor CR (1993). Antigen retrieval technique utilizing citrate buffer or urea solution for immunohistochemical demonstration of androgen receptor in formalin-fixed paraffin sections. J Histochem Cytochem 41 (11): 1599-604.
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
FAQs for CNPase Antibody - BSA Free
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Q: According to datasheet, this product contains sodium azide, so please tell the exact concentration. Because in Japan sodium azide is toxic over 0.1%.
A: The CNPase Antibody (NB100-1935) contains 0.25ml of peptide affinity purified chicken antisera in PBS, pH 7.2 with 0.02% sodium azide preservative.