Anti-MST antibody [EPR29168-60] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
- KO Validated
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Knockout Tested Rabbit Recombinant Monoclonal MST antibody. Carrier free. Suitable for Dot, ICC/IF, Flow Cyt (Intra), IP, WB, IHC-P and reacts with Recombinant fragment - Human, Human, Mouse, Rat samples.
View Alternative Names
TST2, MPST, 3-mercaptopyruvate sulfurtransferase, MST
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling MST with ab317833 at 1/5000 (0.102 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human colon. The section was incubated with ab317833 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 10 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized MPST (MST) KO HEK-293T (MPST(MST) knockout human embryonic kidney epithelial cell), ab266789 cells labelling MST with ab317833 at 1/500 (1.018 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing mainly cytoplasmic staining in wildtype HEK-293T cells and negative staining in MPST (MST) knockout HEK-293T cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Wild-type HEK293T (human embryonic kidney epithelial cell, Left) / MPST(MST) knockout HEK293T (Right) cells labelling MST with ab317833 at 1/500 dilution (0.1 ug)/Red (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling MST with ab317833 at 1/5000 (0.102 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human liver. The section was incubated with ab317833 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 10 mins
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized A431 (human epidermoid carcinoma epithelial cell) cells labelling MST with ab317833 at 1/500 dilution (0.1 ug)/Red (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized A431 (human epidermoid carcinoma epithelial cell) cells labelling MST with ab317833 at 1/500 (1.018 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green).
Confocal image showing mainly cytoplasmic staining in A431 cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
MST was immunoprecipitated from 0.35 mg 293T (human embryonic kidney epithelial cell) whole cell lysate with ab317833 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab317833 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : 293T (human embryonic kidney epithelial cell) whole cell lysate
Lane 2 : ab317833 IP in 293T (human embryonic kidney epithelial cell) whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab317833 in 293T whole cell lysate
All lanes:
Immunoprecipitation - Anti-MST antibody [EPR29168-60] (<a href='/en-us/products/primary-antibodies/mst-antibody-epr29168-60-ab317833'>ab317833</a>) at 1/30 dilution
All lanes:
293T (human embryonic kidney epithelial cell) whole cell lysate with NFDM/TBST
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 24s
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling MST with ab317833 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse liver (PMID : 27973427). The section was incubated with ab317833 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 10 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling MST with ab317833 at 1/2000 (0.255 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat liver. The section was incubated with ab317833 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 10 mins
- WB
Supplier Data
Western blot - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
The samples were run on a Bis-Tris gel under reducing conditions.
Western blot : Anti-MST antibody (ab317833) staining at 1/1000 dilution, shown in green; Mouse anti-alpha Tubulin antibody [DM1A] (ab7291) loading control staining at 1/20, 000 dilution, shown in magenta.
In Western blot, ab317833 was shown to bind specifically to MST. Target of interest was observed at 33 kDa and 35 KDa in wild-type HEK-293T cell lysates (lane 1) with no signal observed at these sizes in MPST (MST) knockout cell line (lane 2, knockout cell line ab266789 / knockout cell lysate ab258524). To generate this image, samples were first run on an SDS-PAGE gel then transferred onto an immobilon-FL PVDF membrane. Membranes were blocked in a fluorescent western blot (TBS-based) blocking solution before incubation with primary antibodies overnight at 4 °C. Blots were washed in TBS-T, incubated with secondary antibodies Goat anti-Rabbit IgG H&L 800CW and Goat anti-Mouse IgG H&L 680RD at 1/20000 dilution for 1 h at room temperature, washed again then imaged.
All lanes:
Western blot - Anti-MST antibody [EPR29168-60] (<a href='/en-us/products/primary-antibodies/mst-antibody-epr29168-60-ab317833'>ab317833</a>) at 1/1000 dilution
Lane 1:
Wild-type HEK-293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg with Intercept® (TBS) Blocking Buffer diluted with an equal volume of 0.1% TBS
Lane 2:
MPST (MST) knockout HEK-293T whole cell lysate at 20 µg with Intercept® (TBS) Blocking Buffer diluted with an equal volume of 0.1% TBS
Lane 3:
HT-29 (human colorectal adenocarcinoma epithelial cell) whole cell lysate at 20 µg with Intercept® (TBS) Blocking Buffer diluted with an equal volume of 0.1% TBS
Lane 4:
A431 (human epidermoid carcinoma epithelial cell) whole cell lysate at 20 µg with Intercept® (TBS) Blocking Buffer diluted with an equal volume of 0.1% TBS
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: 33 kDa,35 kDa
false
- WB
Supplier Data
Western blot - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Low expression : MOLT-4 (PMID : 35204649).
The identity of the lower MW band at approximately 27 kDa (in lane 1) is unknown.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-MST antibody [EPR29168-60] (<a href='/en-us/products/primary-antibodies/mst-antibody-epr29168-60-ab317833'>ab317833</a>) at 1/1000 dilution
Lane 1:
Human lung tissue lysate at 20 µg with NFDM/TBST
Lane 2:
K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate at 20 µg with NFDM/TBST
Lane 3:
MOLT-4 (human lymphoblastic leukemia t lymphoblast) whole cell lysate at 20 µg with NFDM/TBST
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 33 kDa,35 kDa,36 kDa
false
Exposure time: 3s
- WB
Supplier Data
Western blot - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Low expression : lung (PMID : 29712741).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
Exposure time : Lanes 1-5 : 1 second; Lanes 6-8 : 3 seconds.
All lanes:
Western blot - Anti-MST antibody [EPR29168-60] (<a href='/en-us/products/primary-antibodies/mst-antibody-epr29168-60-ab317833'>ab317833</a>) at 1/1000 dilution
Lane 1:
Mouse liver tissue lysate at 20 µg with NFDM/TBST
Lane 2:
Mouse lung tissue lysate at 20 µg with NFDM/TBST
Lane 3:
Mouse brain tissue lysate at 20 µg with NFDM/TBST
Lane 4:
Rat liver tissue lysate at 20 µg with NFDM/TBST
Lane 5:
Rat lung tissue lysate at 20 µg with NFDM/TBST
Lane 6:
F9 (mouse embryonal carcinoma epithelial cell) whole cell lysate at 20 µg with NFDM/TBST
Lane 7:
mIMCD3 (mouse inner medullary collecting duct epithelial cell) whole cell lysate at 20 µg with NFDM/TBST
Lane 8:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 20 µg with NFDM/TBST
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 33 kDa,35 kDa,36 kDa
false
- Dot
Supplier Data
Dot Blot - Anti-MST antibody [EPR29168-60] - BSA and Azide free (AB317834)
This data was developed using ab317833, the same antibody clone in a different buffer formulation.
Dot blot analysis of MST using ab317833 at 1 : 1000 (0.509 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with human TST.
Anti-His tag® antibody (1 : 10000) as total protein control.
All lanes:
Dot Blot - Anti-MST antibody [EPR29168-60] (<a href='/en-us/products/primary-antibodies/mst-antibody-epr29168-60-ab317833'>ab317833</a>) at 1/1000 dilution
Lane 1:
His-tagged human MST fragment
Lane 2:
His-tagged human TST fragment
Secondary
All lanes:
Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
false
Exposure time: 3s
Related conjugates and formulations (1)
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Anti-MST antibody [EPR29168-60]
Reactivity data
Product details
ab317834 is the carrier-free version of ab317833.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
MST plays a significant role in the regulation of the Hippo signaling pathway particularly as a core component of the MST kinase complex. This complex interacts with several other proteins to control organ size and suppress tumor development by regulating the balance between cell division and apoptosis. MST kinases exert influence on cell cycle checkpoints and promote cellular apoptosis aiding in the maintenance of tissue homeostasis.
Pathways
MST proteins are essential within the Hippo signaling pathway and are integrally involved in modulating the MAPK pathway. MST interacts with proteins like LATS1/2 activating them to help mediate the phosphorylation of downstream effectors including YAP and TAZ in the Hippo pathway. These interactions lead to transcriptional changes that govern cell proliferation and apoptosis highlighting MST's role in ensuring proper cellular responses to external and internal stimuli.
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