Rabbit Recombinant Monoclonal ALPK1 antibody. Suitable for WB and reacts with Human samples. Cited in 1 publication.
Preservative: 0.01% Sodium azide
Constituents: 59.94% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
ICC/IF | IP | WB | IHC-P | Flow Cyt (Intra) | |
---|---|---|---|---|---|
Human | Not recommended | Not recommended | Tested | Not recommended | Not recommended |
Mouse | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Rat | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/500 | Notes To get stronger band in western blot, we recommend using freshly made lysate to avoid degradation. Use SDS loading buffer to scrape cell from cell culture plate and boil cell lysate 10 minutes immediately. Incubate primary antibody for 3 hours at room temperature room and incubate secondary antibody overnight. Use higher sensitivity ECL substrate and exposure for longer time. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Serine/threonine-protein kinase that detects bacterial pathogen-associated molecular pattern metabolites (PAMPs) and initiates an innate immune response, a critical step for pathogen elimination and engagement of adaptive immunity (PubMed:28222186, PubMed:28877472, PubMed:30111836). Specifically recognizes and binds ADP-D-glycero-beta-D-manno-heptose (ADP-Heptose), a potent PAMP present in all Gram-negative and some Gram-positive bacteria (PubMed:30111836). ADP-Heptose-binding stimulates its kinase activity to phosphorylate and activate TIFA, triggering pro-inflammatory NF-kappa-B signaling (PubMed:30111836). May be involved in monosodium urate monohydrate (MSU)-induced inflammation by mediating phosphorylation of unconventional myosin MYO9A (PubMed:27169898). May also play a role in apical protein transport by mediating phosphorylation of unconventional myosin MYO1A (PubMed:15883161). May play a role in ciliogenesis (PubMed:30967659).
KIAA1527, LAK, ALPK1, Alpha-protein kinase 1, Chromosome 4 kinase, Lymphocyte alpha-protein kinase
Rabbit Recombinant Monoclonal ALPK1 antibody. Suitable for WB and reacts with Human samples. Cited in 1 publication.
Preservative: 0.01% Sodium azide
Constituents: 59.94% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The image was kindly provided by our collaborator Dr Feng Shao's lab, NIBS.
ab236626 Anti-ALPK1 antibody [EPR20911-169] was shown to react with ALPK1 in 293T cells in Western blot. Loss of signal was observed when ALPK1 knockout sample was used. Wild-type and ALPK1 knockout samples were subjected to SDS-PAGE. ab236626 was incubated 1 hour at room temperature at 1/1000 dilution . Blots were developed with Donkey Anti-Rabbit IgG, (H+L), Peroxidase conjugated secondary antibody at 1/5000 dilution for 1 hour at room temperature before imaging. Anti-beta Tubulin was used as loading control.
Exposure time: 5 minutes
All lanes: Western blot - Anti-ALPK1 antibody [EPR20911-169] (ab236626) at 1/500 dilution
Lane 1: ALPK1 knockout 293T (human embryonic kidney epithelial cell) whole cell lysate at 10 µg
Lane 2: Wild-type 293T whole cell lysate at 10 µg
Lane 3: A549 (human lung carcinoma epithelial cell) whole cell lysate at 20 µg
All lanes: Donkey Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/5000 dilution
Predicted band size: 139 kDa
Observed band size: 140 kDa
Blocking and Diluting buffer: 5% NFDM /TBST.
To get satisfied result, the following protocol tips are strongly recommended. Scrap the cells from cell culture flasks with SDS loading buffer and boil them for 10 minutes immediately. Then prepare membranes with this freshly made lysate. Incubate the membrane with ab236626 at the dilution of 1/500 for 3 hours at room temperature and then secondary antibody Goat Anti-Rabbit IgG H&L (HRP) ab97051 at the dilution of 1/20000 overnight. Acquire WB image with ECL substrate of high sensitivity.
All lanes: Western blot - Anti-ALPK1 antibody [EPR20911-169] (ab236626) at 1/500 dilution
Lane 1: Fresh 293T (human embryonic kidney epithelial cell) whole cell lysate at 40 µg
Lane 2: Fresh A549 (Human lung carcinoma epithelial cell) whole cell lysate at 40 µg
Predicted band size: 139 kDa
Observed band size: 140 kDa
Exposure time: 180s
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