Anti-PHKA1 antibody [EPR12118]
- RabMAb
- Recombinant
- KO Validated
- What is this?
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(2 Publications)
Knockout Tested Rabbit Recombinant Monoclonal PHKA1 antibody. Suitable for IHC-P, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 2 publications.
View Alternative Names
PHKA, PHKA1, Phosphorylase kinase alpha M subunit
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PHKA1 antibody [EPR12118] (AB176338)
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labeling PHKA1 with ab176338 at 1/100 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-PHKA1 antibody [EPR12118] (AB176338)
Intracellular flow cytometric analysis of permeabilized Hela cells labeling PHKA1 with ab176338 at 1/10 dilution (red) or a rabbit IgG (negative) (green).
- WB
Lab
Western blot - Anti-PHKA1 antibody [EPR12118] (AB176338)
False colour image of Western blot : Anti-PHKA1 antibody [EPR12118] staining at 1/1000 dilution, shown in green; Mouse anti-Alpha Tubulin [DM1A] (ab7291) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab176338 was shown to bind specifically to PHKA1. A band was observed at 130 kDa in wild-type HEK-293T cell lysates with no signal observed at this size in PHKA1 knockout cell line ab267337 (knockout cell lysate ab258111). To generate this image, wild-type and PHKA1 knockout HEK-293T cell lysates were analysed. First, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 5 % milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged. Secondary antibodies used were Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution.
Lanes 1 - 2:
Western blot - Anti-PHKA1 antibody [EPR12118] - BSA and Azide free (<a href='/en-us/products/primary-antibodies/phka1-antibody-epr12118-bsa-and-azide-free-ab249913'>ab249913</a>) at 1/1000 dilution
Lanes 1 - 2:
Western blot - Anti-PHKA1 antibody [EPR12118] (ab176338) at 1/1000 dilution
Lane 1:
Wild-type HEK-293T cell lysate at 20 µg
Lane 2:
PHKA1 knockout HEK-293T cell lysate at 20 µg
Lane 2:
Western blot - Human PHKA1 knockout HEK-293T cell line (<a href='/en-us/products/cell-lines/human-phka1-knockout-hek-293t-cell-line-ab267337'>ab267337</a>)
Lane 2:
Western blot - Human PHKA1 knockout HEK-293T cell lysate (<a href='/en-us/products/cell-lysates/human-phka1-knockout-hek-293t-cell-lysate-ab258111'>ab258111</a>)
Secondary
All lanes:
Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution
Observed band size: 130 kDa
false
- WB
Supplier Data
Western blot - Anti-PHKA1 antibody [EPR12118] (AB176338)
All lanes:
Western blot - Anti-PHKA1 antibody [EPR12118] (ab176338) at 1/1000 dilution
Lane 1:
A431 cell lysate at 10 µg
Lane 2:
Jurkat cell lysate at 10 µg
Lane 3:
HeLa cell lysate at 10 µg
Lane 4:
Human skeletal muscle lysate at 10 µg
Predicted band size: 137 kDa
false
Related conjugates and formulations (1)
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Anti-PHKA1 antibody [EPR12118] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Glycogen metabolism involves PHKA1 as part of the phosphorylase kinase complex. This complex exists in the muscle and liver and includes alpha beta gamma and delta subunits. PHKA1 binds together with these subunits to form a large complex helping to regulate the activity state of the enzyme. The regulation of glycogen phosphorylase is important for maintaining energy supply in cells particularly during physical activity.
Pathways
The activity of PHKA1 impacts glycogenolysis which is a significant metabolic pathway responsible for breaking down glycogen into glucose-1-phosphate. This pathway involves other proteins like glycogen phosphorylase and phosphoprotein phosphatase 1. PHKA1 has interactions within the cascade that ensures proper glycogen breakdown especially during conditions requiring increased energy output.
Product protocols
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Target data
Publications (2)
Recent publications for all applications. Explore the full list and refine your search
Carbohydrate polymers 243:116435 PubMed32532388
2020
Applications
Unspecified application
Species
Unspecified reactive species
American journal of physiology. Regulatory, integr 311:R307-14 PubMed27280431
2016
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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