Anti-PKLR antibody [EPR11093] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal PKLR antibody. Carrier free. Suitable for IHC-P, WB and reacts with Human, Mouse, Rat samples.
View Alternative Names
PK1, PKL, PKLR, Pyruvate kinase PKLR, Pyruvate kinase 1, Pyruvate kinase isozymes L/R, R-type/L-type pyruvate kinase, Red cell/liver pyruvate kinase
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation.
Immunohistochemistry of paraffin-embedded Human liver tissue labeling PKLR using ab171744 at 1/250 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation.
Immunohistochemistry of paraffin-embedded Human kidney tissue labeling PKLR using ab171744 at 1/250 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation. Immunohistochemistry analysis of paraffin-embedded human skeletal muscle tissue sections labeling PKLR with ab171744 at 1/250 dilution, incubated for 30 mins at room temperature followed by Goat Anti-Rabbit IgG H&L (HRP), ready to use. Sections were counterstained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Negative control : no staining on human skeletal muscle.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation. Immunohistochemistry analysis of paraffin-embedded human liver tissue sections labeling PKLR with ab171744 at 1/250 dilution, incubated for 30 mins at room temperature followed by Goat Anti-Rabbit IgG H&L (HRP), ready to use. Sections were counterstained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The immunostaining was performed on a Leica Biosystems BOND® RX instrument
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation. Immunohistochemistry analysis of paraffin-embedded rat cardiac muscle tissue sections labeling PKLR with ab171744 at 1/250 dilution, incubated for 30 mins at room temperature followed by Goat Anti-Rabbit IgG H&L (HRP), ready to use. Sections were counterstained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Negative control : no staining on rat cardiac muscle.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation. Immunohistochemistry analysis of paraffin-embedded mouse skeletal muscle tissue sections labeling PKLR with ab171744 at 1/250 dilution, incubated for 30 mins at room temperature followed by Goat Anti-Rabbit IgG H&L (HRP), ready to use. Sections were counterstained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Negative control : no staining on mouse skeletal muscle.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation. Immunohistochemistry analysis of paraffin-embedded rat liver tissue sections labeling PKLR with ab171744 at 1/250 dilution, incubated for 30 mins at room temperature followed by Goat Anti-Rabbit IgG H&L (HRP), ready to use. Sections were counterstained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The immunostaining was performed on a Leica Biosystems BOND® RX instrument.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation. Immunohistochemistry analysis of paraffin-embedded mouse liver tissue sections labeling PKLR with ab171744 at 1/250 dilution, incubated for 30 mins at room temperature followed by Goat Anti-Rabbit IgG H&L (HRP), ready to use. Sections were counterstained with Hematoxylin. Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins. The immunostaining was performed on a Leica Biosystems BOND® RX instrument
- WB
Supplier Data
Western blot - Anti-PKLR antibody [EPR11093] - BSA and Azide free (AB249648)
This data was developed using ab171744, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-PKLR antibody [EPR11093] (<a href='/en-us/products/primary-antibodies/pklr-antibody-epr11093-ab171744'>ab171744</a>) at 1/1000 dilution
Lane 1:
HT-29 cell lysate at 10 µg
Lane 2:
HeLa cell lysate at 10 µg
Lane 3:
HepG2 cell lysate at 10 µg
Lane 4:
293T cell lysate at 10 µg
Predicted band size: 62 kDa
false
Related conjugates and formulations (1)
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Anti-PKLR antibody [EPR11093]
Reactivity data
Product details
ab249648 is the carrier-free version of ab171744.
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
Pyruvate kinase is important for energy production by regulating glycolysis. It exists as a homo-tetramer forming a complex to execute its enzymatic activity. This complex ensures the efficient conversion of PEP facilitating the flow of carbon through the glycolytic pathway. In the liver PKLR plays a role in gluconeogenesis and lipogenesis while in red blood cells it contributes directly to ATP production essential for maintaining cellular energy and function.
Pathways
The pyruvate kinase enzyme is a significant participant in glycolysis and gluconeogenesis. These pathways are central to energy metabolism linking glucose breakdown with ATP generation. Pyruvate kinase interacts with enzymes like hexokinase and phosphofructokinase within the glycolytic pathway coordinating with these enzymes to regulate energy metabolism. In gluconeogenesis PKLR integrates into the mechanism ensuring the balance between energy production and storage.
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