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BRAND / VENDOR: Abcam

Abcam, ab30554, Anti-14-3-3 (phospho S58) antibody

CATALOG NUMBER: ab30554
السعر العادي$0.99
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Product Description

Size: 50µL
Rabbit Polyclonal 1433B phospho S58 antibody. Suitable for WB, IHC-Fr and reacts with Mouse, Rat, Zebrafish samples. Cited in 3 publications. Immunogen corresponding to Synthetic Peptide within Human YWHAB phospho S58.
Key facts
Host species:Rabbit,
Clonality:Polyclonal,
Isotype:IgG,
Carrier free:No,
Reacts with:Mouse, Rat, Zebrafish,
Applications:WB, IHC-FrSee reactivity dataSee the reactivity data table below for information on validated species and application combinations.,
Immunogen:Synthetic Peptide within Human YWHAB phospho S58. The exact immunogen used to generate this antibody is proprietary information.P31946,
Specificity:Specific for the ~29k 14-3-3 protein phosphorylated at Ser58. Immunolabeling is blocked by the phosphopeptide used as antigen but not by the corresponding dephosphopeptide.The N-terminal sequence used as antigen has high homology across a wide variety of species for all of the 14-3-3 proteins. We have not specifically tested it for reactivity against each protein in any given species, we do expect it to recognize most all of them.

Properties and Storage Information:
Form-Liquid, Purification technique-Affinity purification Immunogen, Purification notes-Prepared from rabbit serum by affinity purification via sequentialchromatography on phospho- and dephosphopeptide affinity columns., Storage buffer-pH: 7.5Constituents: 50% Glycerol (glycerin, glycerine), 0.87% Sodium chloride, 0.238% HEPES, 0.01% BSA, Shipped at conditions-Blue Ice, Appropriate short-term storage conditions-+4°C, Appropriate long-term storage conditions--20°C, Aliquoting information-Upon delivery aliquot, Storage information-Avoid freeze / thaw cycle

Supplementary Information:
This supplementary information is collated from multiple sources and compiled automatically.
The 14-3-3 proteins are a family of regulatory molecules with a molecular mass around 28 to 32 kDa. These proteins exist in seven isoforms in humans termed beta gamma epsilon zeta eta theta and sigma. 14-3-3 proteins are ubiquitously expressed in eukaryotic cells including neurons liver cells and immune cells. These proteins participate in modulation of many cellular processes by binding to phosphorylated serine and threonine residues on various target proteins. This binding alters the conformation of target proteins influencing their activity subcellular localization or stability.
Biological function summary
14-3-3 proteins are involved in signal transduction cell cycle control and apoptosis regulation. They participate in protein interactions and form dimers that serve as scaffolds assembling complexes and linking signaling pathways. The proteins associate with kinases such as Raf-1 thereby contributing to signaling pathways that include MAPK/ERK. At the cellular level 14-3-3 proteins govern key mechanisms like the G1/S phase transition and stress response which are critical for maintaining cellular homeostasis.
Pathways
14-3-3 proteins play critical roles in the PI3K/AKT and MAPK/ERK pathways. They interact with several key proteins within these pathways including AKT and Raf-1 mediating cellular responses to growth factors and stress. In the PI3K/AKT pathway 14-3-3 proteins help regulate the progression of the cell cycle and promote cell survival linking extracellular signals to the machinery that governs cell fate. These interactions underline the role of 14-3-3 proteins in integrating and regulating complex cell signaling networks.
14-3-3 proteins are associated with neurodegenerative diseases like Alzheimer's and certain types of cancer. In Alzheimer's disease 14-3-3 proteins interact with tau protein contributing to the pathological aggregation of tau associated with neuronal damage. Similarly in various cancers their interaction with cell cycle regulators like p53 can influence tumor progression by affecting cell division and apoptosis. These connections highlight the involvement of 14-3-3 proteins in disease mechanisms making them potential targets for therapeutic intervention.


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Collaboration

Tony Tang

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