Rabbit Recombinant Multiclonal STAM1 antibody. Suitable for WB and reacts with Human, Mouse samples. Immunogen corresponding to Synthetic Peptide within Human STAM.
Preservative: 0.09% Sodium azide
Constituents: 99.91% PBS
WB | |
---|---|
Human | Tested |
Mouse | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 2-2.5 µg/mL | Notes - |
Species Mouse | Dilution info 2.5 µg/mL | Notes - |
Involved in intracellular signal transduction mediated by cytokines and growth factors. Upon IL-2 and GM-CSL stimulation, it plays a role in signaling leading to DNA synthesis and MYC induction. May also play a role in T-cell development. Involved in down-regulation of receptor tyrosine kinase via multivesicular body (MVBs) when complexed with HGS (ESCRT-0 complex). The ESCRT-0 complex binds ubiquitin and acts as a sorting machinery that recognizes ubiquitinated receptors and transfers them to further sequential lysosomal sorting/trafficking processes. (Microbial infection) Plays an important role in Dengue virus entry.
STAM1, STAM, Signal transducing adapter molecule 1, STAM-1
Rabbit Recombinant Multiclonal STAM1 antibody. Suitable for WB and reacts with Human, Mouse samples. Immunogen corresponding to Synthetic Peptide within Human STAM.
Preservative: 0.09% Sodium azide
Constituents: 99.91% PBS
What are recombinant multiclonals?
Recombinant multiclonals are a mixture of recombinant antibodies co-expressed from a library of heavy and light chains. They offer several advantages including:
View our range of recombinant multiclonal antibodies.
STAM or Signal Transducing Adaptor Molecule is a protein involved in intracellular signaling pathways. It is also known by the alternate name STAM-1 and has a mass of approximately 55 kDa. STAM is expressed in various tissues with a significant presence in the immune and hematopoietic systems. Its mechanical role involves interacting with different cellular components to facilitate signal transduction. The protein mainly localizes to the cytoplasm and occasionally associates with membrane-bound organelles.
STAM engages in processes that are essential for signal transduction and endosomal sorting. It works as part of a larger protein complex known as the ESCRT-0 complex which is important for regulating endocytosis and sorting of ubiquitinated membrane proteins. This complex includes other proteins such as Hrs and plays a role in the degradation of signaling receptors assisting in modulating cell signaling and maintaining cellular equilibrium.
STAM is implicated in the endocytic and ubiquitin-proteasome systems. It interacts significantly with the endocytosis pathway participating in the sorting of endocytic vesicles. In this context STAM's function involves cooperation with proteins like Hrs in the ESCRT machinery which manages membrane receptor recycling and degradation. By controlling these pathways it modulates signal transduction and influences cell fate decisions.
STAM's dysfunction is linked to certain conditions including cancer and neurodegenerative diseases. In cancer aberrant STAM function can result in uncontrolled cellular proliferation as seen with its association with proteins such as c-MET a receptor tyrosine kinase. In neurodegenerative diseases malfunction of STAM can disrupt cellular homeostasis and protein degradation pathways contributing to neuronal cell death. Understanding STAM's interactions and pathways can provide insights into potential therapeutic targets for these diseases.
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Western blot analysis of STAM in whole cell extracts from mouse brain using ab308114 at a dilution of 2.5 µg/mL. Detection was performed using an HRP-conjugated Goat anti-Rabbit secondary antibody followed by chemiluminescence (ECL). Results show a band at ~58kDa.
All lanes: Western blot - Anti-STAM antibody [RP23040090] (ab308114) at 2.5 µg/mL
All lanes: Mouse brain whole cell extracts
All lanes: HRP-conjugated Goat anti-Rabbit secondary antibody
Developed using the ECL technique.
Observed band size: 58 kDa
Western blot analysis was performed on whole cell extracts of Caco-2 (Lane 1), A431 (Lane 2), A-375 (Lane 3), A549 (Lane 4), Caki-1 (Lane 5) and DU 145 (Lane 6). The blots were probed with ab308114, 2µg/mL and detected by chemiluminescence using Goat anti-Rabbit IgG (H+L) Secondary Antibody, HRP conjµgate (0.4µg/mL, 1:2500 dilution). A ~ 60 kDa band corresponding to STAM was observed across all cell lines tested. Known quantity of protein samples were electrophoresed using a 4-12% Bis-Tris gel, electrophoresis system and pre-stained protein standard. Resolved proteins were then transferred onto a nitrocellulose membrane. The membrane was probed with the relevant primary and secondary Antibody following blocking with 5 % skimmed milk. Chemiluminescent detection was performed (ECL).
All lanes: Western blot - Anti-STAM antibody [RP23040090] (ab308114) at 2 µg/mL
Lane 1: Caco-2 whole cell extract
Lane 2: A431 whole cell extract
Lane 3: A-375 whole cell extract
Lane 4: A549 whole cell extract
Lane 5: Caki-1 whole cell extract
Lane 6: DU-145 whole cell extract
All lanes: Goat anti Rabbit IgG (H+L) Secondary Antibody, HRP conjµgate at 1/2500 dilution
Developed using the ECL technique.
Predicted band size: 58 kDa
Observed band size: 60 kDa
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