KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free
Novus Biologicals | Catalog # NBP1-80270
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Key Product Details
Species Reactivity
Human
Applications
Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot
Label
Unconjugated
Antibody Source
Polyclonal Rabbit IgG
Format
BSA Free
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Product Specifications
Immunogen
Synthetic peptide directed towards the middle region of human GRIK5. Peptide sequence EDGLYGAPEPNGSWTGMVGELINRKADLAVAAFTITAEREKVIDFSKPFM. The peptide sequence for this immunogen was taken from within the described region.
Clonality
Polyclonal
Host
Rabbit
Isotype
IgG
Description
The addition of 50% glycerol is optional for those storing this antibody at -20C and not aliquoting smaller units. However, please note that glycerol may interrupt some downstream antibody applications and should be added with caution.
Scientific Data Images for KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free
Western Blot: KA2/GRIK5/Glutamate Receptor KA2 Antibody [NBP1-80270]
Western Blot: KA2/GRIK5/Glutamate Receptor KA2 Antibody [NBP1-80270] - Jurkat cell lysate. Suggested Antibody Titration: 0.2 - 1 ug/mL.Immunohistochemistry-Paraffin: KA2/GRIK5/Glutamate Receptor KA2 Antibody [NBP1-80270] -
Immunohistochemistry-Paraffin: KA2/GRIK5/Glutamate Receptor KA2 Antibody [NBP1-80270] - FFPE Human Pineal Tissue. Primary antibody at 1:100.Immunohistochemistry: KA2/GRIK5/Glutamate Receptor KA2 Antibody [NBP1-80270] -
Immunohistochemistry: KA2/GRIK5/Glutamate Receptor KA2 Antibody [NBP1-80270] - Mouse Retina, 25 ug/mL.Western Blot: KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free [NBP1-80270] -
Altered abundance of glutamate receptor subunits in HPC synaptosomes from Dp1Tyb, Dp(17)3Yey, and Dp(10)2Yey male mice. (A–C) HPC synaptosomes from the indicated mouse strains were analyzed by immunoblotting for glutamate receptor subunits and PSD95. Example immunoblots are shown on the left and mean +/- SEM protein abundance on the right, normalized to beta -actin (or to GluA1 or GluN2B in case of phosphorylation levels of the respective receptor) and then to the mean signal in WT mice. Immunoblots show analysis of HPC synaptosome extracts from 2 to 5 mice of each genotype. Compared to WT littermates, mutant Dp1Tyb mice displayed lower hippocampal expression of GluA1, pGluA1(S845), and PSD95 (Student’s t-test, *p < 0.05) (A). Mutant Dp(10)2Yey mice displayed an age-dependent decrease in hippocampal expression of GluK5 and PSD95 compared to WT littermates (two-way ANOVA, *p < 0.05, **p < 0.001) (C). The decrease in GluK5 expression was not driven by age-dependent changes in the WT group as this comparison was not statistically significant (p > 0.05) (C). 21-month-old Dp1Tyb: n = 6 WT, 5 Dp1Tyb; 21-month-old Dp(17)3Yey: n = 9 WT, 12 Dp(17)3Yey; 14-month-old Dp(10)2Yey: n = 9 WT, 11 Dp(10)2Yey; 22-month-old Dp(10)2Yey: n = 6 WT, 10 Dp(10)2Yey. Image collected and cropped by CiteAb from the following open publication (https://www.frontiersin.org/articles/10.3389/fnbeh.2024.1428146/full), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free [NBP1-80270] -
Altered abundance of glutamate receptor subunits in HPC synaptosomes from Dp1Tyb, Dp(17)3Yey, and Dp(10)2Yey male mice. (A–C) HPC synaptosomes from the indicated mouse strains were analyzed by immunoblotting for glutamate receptor subunits and PSD95. Example immunoblots are shown on the left and mean +/- SEM protein abundance on the right, normalized to beta -actin (or to GluA1 or GluN2B in case of phosphorylation levels of the respective receptor) and then to the mean signal in WT mice. Immunoblots show analysis of HPC synaptosome extracts from 2 to 5 mice of each genotype. Compared to WT littermates, mutant Dp1Tyb mice displayed lower hippocampal expression of GluA1, pGluA1(S845), and PSD95 (Student’s t-test, *p < 0.05) (A). Mutant Dp(10)2Yey mice displayed an age-dependent decrease in hippocampal expression of GluK5 and PSD95 compared to WT littermates (two-way ANOVA, *p < 0.05, **p < 0.001) (C). The decrease in GluK5 expression was not driven by age-dependent changes in the WT group as this comparison was not statistically significant (p > 0.05) (C). 21-month-old Dp1Tyb: n = 6 WT, 5 Dp1Tyb; 21-month-old Dp(17)3Yey: n = 9 WT, 12 Dp(17)3Yey; 14-month-old Dp(10)2Yey: n = 9 WT, 11 Dp(10)2Yey; 22-month-old Dp(10)2Yey: n = 6 WT, 10 Dp(10)2Yey. Image collected and cropped by CiteAb from the following open publication (https://www.frontiersin.org/articles/10.3389/fnbeh.2024.1428146/full), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Western Blot: KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free [NBP1-80270] -
Altered abundance of glutamate receptor subunits in HPC synaptosomes from Dp1Tyb, Dp(17)3Yey, and Dp(10)2Yey male mice. (A–C) HPC synaptosomes from the indicated mouse strains were analyzed by immunoblotting for glutamate receptor subunits and PSD95. Example immunoblots are shown on the left and mean +/- SEM protein abundance on the right, normalized to beta -actin (or to GluA1 or GluN2B in case of phosphorylation levels of the respective receptor) and then to the mean signal in WT mice. Immunoblots show analysis of HPC synaptosome extracts from 2 to 5 mice of each genotype. Compared to WT littermates, mutant Dp1Tyb mice displayed lower hippocampal expression of GluA1, pGluA1(S845), and PSD95 (Student’s t-test, *p < 0.05) (A). Mutant Dp(10)2Yey mice displayed an age-dependent decrease in hippocampal expression of GluK5 and PSD95 compared to WT littermates (two-way ANOVA, *p < 0.05, **p < 0.001) (C). The decrease in GluK5 expression was not driven by age-dependent changes in the WT group as this comparison was not statistically significant (p > 0.05) (C). 21-month-old Dp1Tyb: n = 6 WT, 5 Dp1Tyb; 21-month-old Dp(17)3Yey: n = 9 WT, 12 Dp(17)3Yey; 14-month-old Dp(10)2Yey: n = 9 WT, 11 Dp(10)2Yey; 22-month-old Dp(10)2Yey: n = 6 WT, 10 Dp(10)2Yey. Image collected and cropped by CiteAb from the following open publication (https://www.frontiersin.org/articles/10.3389/fnbeh.2024.1428146/full), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free
Application
Recommended Usage
Immunohistochemistry
1:10-1:500
Western Blot
1.0 ug/ml
Formulation, Preparation, and Storage
Purification
Affinity purified
Formulation
PBS, 2% Sucrose
Format
BSA Free
Preservative
0.09% Sodium Azide
Concentration
0.5 mg/ml
Shipping
The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Background: KA2/GRIK5
Long Name
Glutamate Receptor KA2
Alternate Names
EAA2, GluK5, GRIK2, GRIK5
Gene Symbol
GRIK5
UniProt
Additional KA2/GRIK5 Products
Product Documents for KA2/GRIK5/Glutamate Receptor KA2 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 KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free
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.
Related Research Areas
Citations for KA2/GRIK5/Glutamate Receptor KA2 Antibody - BSA Free
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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
- 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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