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AB309547

Anti-TMPRSS2 antibody [P5H9-A3] - BSA and Azide free

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Knockout Tested Mouse Recombinant Monoclonal TMPRSS2 antibody. Carrier free. Suitable for WB, ICC/IF and reacts with Human samples.

View Alternative Names

PRSS10, TMPRSS2, Transmembrane protease serine 2, Serine protease 10

3 Images
Immunocytochemistry/ Immunofluorescence - Anti-TMPRSS2 antibody [P5H9-A3] - BSA and Azide free (AB309547)
  • ICC/IF

Supplier Data

Immunocytochemistry/ Immunofluorescence - Anti-TMPRSS2 antibody [P5H9-A3] - BSA and Azide free (AB309547)

This data was developed using ab309546 the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized LNCaP (human prostate carcinoma epithelial cell) cells labelling TMPRSS2 with ab309546 at 1/100 (10.28 ug/ml) dilution, followed by ab150113 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in LNCaP and negative staining in 293T (PMID : 33493182).Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). ab206369 Anti-beta Tubulin rabbit monoclonal antibody (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue). antibody only control : Secondary antibody is ab150113 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) at 1/1000 dilution.

Western blot - Anti-TMPRSS2 antibody [P5H9-A3] - BSA and Azide free (AB309547)
  • WB

Supplier Data

Western blot - Anti-TMPRSS2 antibody [P5H9-A3] - BSA and Azide free (AB309547)

This data was developed using ab309546, the same antibody clone in a different buffer formulation.

Blocking and diluting buffer and concentration : 5% NFDM/TBST.

Negative control : 293T (PMID : 33493182).

In Western blot, anti- GAPDH antibody (ab181602) loading control staining at 1/200000 dilution.

All lanes:

Western blot - Anti-TMPRSS2 antibody [P5H9-A3] (<a href='/en-us/products/primary-antibodies/tmprss2-antibody-p5h9-a3-ab309546'>ab309546</a>) at 1/1000 dilution

Lane 1:

LNCaP (human prostate carcinoma epithelial cell) whole cell lysate at 20 µg

Lane 2:

293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg

Secondary

All lanes:

Peroxidase-Conjugated Goat anti-Mouse IgG (H+L) at 1/10000 dilution

Observed band size: 25 kDa,55 kDa

false

Exposure time: 15s

Western blot - Anti-TMPRSS2 antibody [P5H9-A3] - BSA and Azide free (AB309547)
  • WB

Supplier Data

Western blot - Anti-TMPRSS2 antibody [P5H9-A3] - BSA and Azide free (AB309547)

This data was developed using ab309546, the same antibody clone in a different buffer formulation.Blocking and diluting buffer and concentration : Intercept® (TBS) Blocking Buffer diluted with an equal volume of TBS Lysates at 20 µg per lane. The samples were run on a Bis-Tris gel under reducing conditions. Western blot : Anti-TMPRSS2 antibody (ab309546) staining at 1/1000 dilution, shown in green; Rabbit anti-GAPDH antibody (ab181602) loading control staining at 1/20000 dilution, shown in red. In Western blot, ab309546 was shown to bind specifically to TMPRSS2. Target of interest was observed at 55 kDa and 25 KDa in wild-type LNCaP cell lysates (lane 1) with no signal observed at this size in TMPRSS2 knockout cell line (lane 2, knockout cell line ab273745). 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. The molecular weight observed is consistent with what has been described in the literature (PMID : 35104687). Exposure time :

All lanes:

Western blot - Anti-TMPRSS2 antibody [P5H9-A3] (<a href='/en-us/products/primary-antibodies/tmprss2-antibody-p5h9-a3-ab309546'>ab309546</a>) at 1/1000 dilution

Lane 1:

Wild-type LNCaP (human prostate carcinoma epithelial cell) whole cell lysate at 20 µg

Lane 2:

TMPRSS2 knockout LNCaP whole cell lysate at 20 µg

Lane 2:

Western blot - Human TMPRSS2 knockout LNCaP cell line (<a href='/en-us/products/cell-lines/human-tmprss2-knockout-lncap-cell-line-ab273745'>ab273745</a>)

Secondary

Lanes 1 - 2:

Western blot - Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-irdye-680rd-preadsorbed-ab216777'>ab216777</a>) at 1/200000 dilution

Lanes 1 - 2:

Western blot - Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (<a href='/en-us/products/secondary-antibodies/goat-mouse-igg-h-l-irdye-800cw-preadsorbed-ab216772'>ab216772</a>) at 1/200000 dilution

Observed band size: 25 kDa,55 kDa

false

Key facts

Host species

Mouse

Clonality

Monoclonal

Clone number

P5H9-A3

Isotype

IgG1

Carrier free

Yes

Reacts with

Human

Applications

ICC/IF, WB

applications

Immunogen

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

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Product details

Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com

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
Liquid
Purification technique
Affinity purification Protein A
Storage buffer
pH: 7.2 - 7.4 Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
+4°C

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Plasma membrane-anchored serine protease that cleaves at arginine residues (PubMed : 32703818, PubMed : 35676539, PubMed : 37990007, PubMed : 38964328). Participates in proteolytic cascades of relevance for the normal physiologic function of the prostate (PubMed : 25122198). Androgen-induced TMPRSS2 activates several substrates that include pro-hepatocyte growth factor/HGF, the protease activated receptor-2/F2RL1 or matriptase/ST14 leading to extracellular matrix disruption and metastasis of prostate cancer cells (PubMed : 15537383, PubMed : 25122198, PubMed : 26018085). In addition, activates trigeminal neurons and contribute to both spontaneous pain and mechanical allodynia (By similarity).. (Microbial infection) Facilitates human coronaviruses SARS-CoV and SARS-CoV-2 infections via two independent mechanisms, proteolytic cleavage of ACE2 receptor which promotes viral uptake, and cleavage of coronavirus spike glycoproteins which activates the glycoprotein for host cell entry (PubMed : 24227843, PubMed : 32142651, PubMed : 32404436, PubMed : 33051876, PubMed : 34159616, PubMed : 35676539, PubMed : 37990007). The cleavage of SARS-COV2 spike glycoprotein occurs between the S2 and S2' site (PubMed : 32703818). Upon SARS-CoV-2 infection, increases syncytia formation by accelerating the fusion process (PubMed : 33051876, PubMed : 34159616, PubMed : 35676539). Proteolytically cleaves and activates the spike glycoproteins of human coronavirus 229E (HCoV-229E) and human coronavirus EMC (HCoV-EMC) and the fusion glycoproteins F0 of Sendai virus (SeV), human metapneumovirus (HMPV), human parainfluenza 1, 2, 3, 4a and 4b viruses (HPIV). Essential for spread and pathogenesis of influenza A virus (strains H1N1, H3N2 and H7N9); involved in proteolytic cleavage and activation of hemagglutinin (HA) protein which is essential for viral infectivity.. (Microbial infection) Receptor for human coronavirus HKU1-CoV, acts synergistically with disialoside glycans to facilitate the entry of the virus. After binding to cell-surface disialoside glycans, the viral S protein interacts with the inactive form of TMPRSS2 and inhibits its protease activity.
See full target information TMPRSS2

Product promise

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