Anti-Stathmin 1 (phospho S63) antibody [EPR1574] - BSA and Azide free
- RabMAb
- Recombinant
- What is this?
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(1 Publication)
Rabbit Recombinant Monoclonal Stathmin 1 phospho S63 antibody. Carrier free. Suitable for IHC-P, IP, Dot, WB and reacts with Human, Synthetic peptide samples. Cited in 1 publication.
View Alternative Names
C1orf215, LAP18, OP18, STMN1, Stathmin, Leukemia-associated phosphoprotein p18, Metablastin, Oncoprotein 18, Phosphoprotein p19, Prosolin, Protein Pr22, pp17, Op18, pp19
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Stathmin 1 (phospho S63) antibody [EPR1574] - BSA and Azide free (AB239888)
ab76583, at a 1/250 dilution, staining Stathmin 1 in paraffin embedded human brain tissue by Immunohistochemistry.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab76583).
Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
- IP
Lab
Immunoprecipitation - Anti-Stathmin 1 (phospho S63) antibody [EPR1574] - BSA and Azide free (AB239888)
This data was developed using ab76583, the same antibody clone in a different buffer formulation.
Stathmin 1 was immunoprecipitated from 0.35 mg HeLa (Human cervix adenocarcinoma epithelial cell) treated with Calyculin A whole cell lysate 10 μg with ab76583 at 1/50 dilution (2μg). VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (Human cervix adenocarcinoma epithelial cell) treated with Calyculin A whole cell lysate 10 μg
Lane 2 : ab76583 IP in HeLa treated with Calyculin A whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab76583 in HeLa treated with Calyculin A whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
75kDa band could be stathmin/alpha tubulin complex. (PMID : 9369201)
All lanes:
Immunoprecipitation - Anti-Stathmin 1 (phospho S63) antibody [EPR1574] (<a href='/en-us/products/primary-antibodies/stathmin-1-phospho-s63-antibody-epr1574-ab76583'>ab76583</a>)
Predicted band size: 17 kDa
Observed band size: 17 kDa
false
- Dot
Unknown
Dot Blot - Anti-Stathmin 1 (phospho S63) antibody [EPR1574] - BSA and Azide free (AB239888)
Dot blot analysis of Stathmin 1 (phospho S63) phospho peptide (Lane 1) and Stathmin 1 non-phospho peptide (Lane 2) labeling Stathmin 1 (phospho S63) with ab76583 at a dilution of 1/1000. ab97051 (Peroxidase conjugated goat anti-rabbit IgG) (H+L) at 1/100 000 was used as the secondary antibody.
Blocking and diluting buffer : 5% NFDM/TBST.
Exposure time : 3 minutes.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab76583).
Related conjugates and formulations (1)
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Anti-Stathmin 1 (phospho S63) antibody [EPR1574]
Reactivity data
Product details
ab239888 is the carrier-free version of ab76583.
Species reactivity
Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species.
Please contact us for more information.
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
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Stathmin 1 is important in cell cycle regulation and cell signaling. It does not operate as part of a larger protein complex but rather exerts its effects directly on microtubules. By overriding the stabilization of microtubules it ensures proper mitotic spindle function. This action is especially significant during the G2/M transition and mitosis contributing to the precise segregation of chromosomes.
Pathways
The regulation of microtubule dynamics by Stathmin 1 plays an important role in cell division and neuronal development. It is involved in the PI3K/AKT signaling pathway which ensures cell survival and proliferation. Stathmin 1 interacts with other regulatory proteins such as Tau which stabilizes microtubules offering a balance between dynamic instability and stabilization. This interaction highlights its involvement in cytoskeletal reorganization essential for both cancer progression and neuronal function.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Frontiers in immunology 13:869365 PubMed35967407
2022
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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