Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
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Rabbit Recombinant Monoclonal GLYR1 antibody. Carrier free. Suitable for IHC-P, WB and reacts with Human, Mouse, Rat samples.
View Alternative Names
HIBDL, NDF, NP60, NPAC, GLYR1, Cytokine-like nuclear factor N-PAC, 3-hydroxyisobutyrate dehydrogenase-like protein, Glyoxylate reductase 1 homolog, Nuclear protein NP60, Nuclear protein of 60 kDa, Nucleosome-destabilizing factor, Putative oxidoreductase GLYR1, hNDF
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
ab167155 showing +ve staining in Human normal brain.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- WB
Lab
Western blot - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
Lanes 1-4 : Merged signal (red and green). Green - ab167155 observed at 61 kDa. Red - loading control ab8245 observed at 36 kDa.
ab167155 Anti-GLYR1 antibody [EPR10077(B)] was shown to specifically react with GLYR1 in wild-type HEK293T cells. Loss of signal was observed when knockout cell line ab266610 (knockout cell lysate ab257968) was used. Wild-type and GLYR1 knockout samples were subjected to SDS-PAGE. ab167155 and Anti-GAPDH antibody [6C5] - Loading Control (ab8245) were incubated overnight at 4°C at 1 in 1000 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
All lanes:
Western blot - Anti-GLYR1 antibody [EPR10077(B)] (<a href='/en-us/products/primary-antibodies/glyr1-antibody-epr10077b-ab167155'>ab167155</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK293T cell lysate at 20 µg
Lane 2:
GLYR1 knockout HEK293T cell lysate at 20 µg
Lane 2:
Western blot - Human GLYR1 knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-glyr1-knockout-hek-293t-cell-line-ab266610'>ab266610</a>)
Lane 3:
HeLa cell lysate at 20 µg
Lane 4:
HUVEC cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-800cw-preadsorbed-ab216773'>ab216773</a>) at 1/10000 dilution
Predicted band size: 61 kDa,68 kDa
Observed band size: 61 kDa
false
- WB
Unknown
Western blot - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-GLYR1 antibody [EPR10077(B)] (<a href='/en-us/products/primary-antibodies/glyr1-antibody-epr10077b-ab167155'>ab167155</a>) at 1/1000 dilution
Lane 1:
Jurkat cell lysate at 10 µg
Lane 2:
HeLa cell lysate at 10 µg
Lane 3:
K562 cell lysate at 10 µg
Predicted band size: 54 kDa,61 kDa
false
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
ab167155 showing +ve staining in Mouse kidney.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
ab167155 showing +ve staining in Human ovarian carcinoma.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
ab167155 showing +ve staining in Human thyroid gland papillary carcinoma.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded Human colon tissue labeling GLYR1 with ab167155 at a 1/50 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLYR1 antibody [EPR10077(B)] - BSA and Azide free (AB249399)
This data was developed using ab167155, the same antibody clone in a different buffer formulation.
ab167155 showing +ve staining in Human normal stomach.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Related conjugates and formulations (1)
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Anti-GLYR1 antibody [EPR10077(B)]
Reactivity data
Product details
ab249399 is the carrier-free version of ab167155.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
GLYR1 influences chromatin structure by regulating histone H3 lysine 36 trimethylation (H3K36me3). It interacts with lysine-specific demethylase 1 (LSD1) and partners within chromatin-modifying complexes. Through these interactions GLYR1 can impact transcriptional repression and activation. Its activity shows specific importance in controlling gene expression related to cell growth and differentiation.
Pathways
GLYR1 interacts with components of the MAPK signaling pathway and the histone modification pathway. It works alongside proteins like LSD1 and histone deacetylases (HDACs) to modulate transcriptional outcomes. These interactions provide evidence of its role in transmitting extracellular signals to the nucleus ultimately influencing gene expression patterns.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com