Anti-SF3B1 antibody [EPR11986] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal SF3B1 antibody. Carrier free. Suitable for IHC-P, WB, ICC/IF, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 1 publication.
View Alternative Names
SAP155, SF3B1, Splicing factor 3B subunit 1, Pre-mRNA-splicing factor SF3b 155 kDa subunit, Spliceosome-associated protein 155, SF3b155, SAP 155
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634). Immunocytochemistry/ Immunofluorescence analysis of HeLa (human cervical adenocarcinoma epithelial cell) labeling SF3B1 with ab172634 at 1/200 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution. Cells were fixed with 4% Paraformaldehyde and permeabilised with 0.1% TritonX-100. Nuclear counterstain was DAPI. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) at 1/200 was used as counterstain antibody. Confocal image showing nuclear staining in Hela cell line. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
Intracellular Flow Cytometry analysis of HeLa (human cervix adenocarcinoma) cells labeling SF3B1 (red) with ab172634 at a 1/2000 dilution. Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol. A goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) was used as the secondary antibody at a 1/2000 dilution. Black - Rabbit monoclonal IgG (ab172730). Blue (unlabeled control) - Cells without incubation with the primary and secondary antibodies.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
Immunohistochemical analysis of Formalin-fixed, paraffin-embedded Human glioma tissue labeling SF3B1 with ab172634 at 1/100 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634).
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
Immunohistochemical analysis of Formalin-fixed, paraffin-embedded Human colon tissue labeling SF3B1 with ab172634 at 1/100 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634).
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
Immunofluorescence analysis of HeLa cells labeling SF3B1 with ab172634 at 1/250 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634). Immunocytochemistry/ Immunofluorescence analysis of NIH/3T3 (mouse embryonic fibroblast) labeling SF3B1 with ab172634 at 1/200 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution. Cells were fixed with 4% Paraformaldehyde and permeabilised with 0.1% TritonX-100. Nuclear counterstain was DAPI. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) at 1/200 was used as counterstain antibody. Confocal image showing nuclear staining in NIH/3T3 cell line. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- WB
Lab
Western blot - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634). Blocking/Diluting buffer and concentration : 5% NFDM/TBST Exposure time : Lane 1-4 : 1 second Lane 5-6 : 10 seconds In Western blot, anti- H3 antibody (ab176842) loading control staining at 1/100000 dilution and anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution.
All lanes:
Western blot - Anti-SF3B1 antibody [EPR11986] (<a href='/en-us/products/primary-antibodies/sf3b1-antibody-epr11986-ab172634'>ab172634</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervical adenocarcinoma epithelial cell) nuclear fraction at 20 µg
Lane 2:
HeLa (human cervical adenocarcinoma epithelial cell) cytoplasmic fraction at 20 µg
Lane 3:
PC-12 (rat adrenal gland pheochromocytoma cell) nuclear fraction at 20 µg
Lane 4:
PC-12 (rat adrenal gland pheochromocytoma cell) cytoplasmic fraction at 20 µg
Lane 5:
RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) nuclear fraction at 20 µg
Lane 6:
RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) cytoplasmic fraction at 20 µg
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: 145 kDa
false
- WB
Lab
Western blot - Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (AB240170)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab172634). Blocking/Diluting buffer and concentration : 5% NFDM/TBST Exposure time : Lane 1-3 : 3.25 seconds Lane 4 : 15 seconds
All lanes:
Western blot - Anti-SF3B1 antibody [EPR11986] (<a href='/en-us/products/primary-antibodies/sf3b1-antibody-epr11986-ab172634'>ab172634</a>) at 1/1000 dilution
Lane 1:
RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate at 20 µg
Lane 2:
PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate at 20 µg
Lane 3:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 4:
C6 (rat glial tumor glial cell) whole cell lysate at 20 µg
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: 146 kDa
false
Related conjugates and formulations (9)
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Anti-SF3B1 antibody [EPR11986]
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660 APC
APC Anti-SF3B1 antibody [EPR11986]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-SF3B1 antibody [EPR11986]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-SF3B1 antibody [EPR11986]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-SF3B1 antibody [EPR11986]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-SF3B1 antibody [EPR11986]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-SF3B1 antibody [EPR11986]
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HRP Anti-SF3B1 antibody [EPR11986]
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578 PE
PE Anti-SF3B1 antibody [EPR11986]
Reactivity data
Product details
ab240170 is the carrier-free version of ab172634.
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
SF3B1 is an essential component of the spliceosomal complex specifically the U2 snRNP component. It helps establish the branchpoint recognition complex ensuring accurate RNA splicing necessary for producing functional mRNA molecules. This process is important for the expression of diverse protein-coding genes affecting multiple aspects of cellular function and identity. The protein interacts with other spliceosomal proteins like SF3A and U2AF to guide the precise removal of non-coding sequences enabling proper translation into proteins.
Pathways
SF3B1 is involved in the mRNA processing pathway and influences the cell cycle pathway. During mRNA processing SF3B1 aids in assembling the spliceosome facilitating the excision of introns. The protein interacts with components like SF3B2 in coordinating splicing with other RNA processing events. In the cell cycle pathway SF3B1 indirectly affects gene expression and stability influencing cell cycle progression and serving as a regulatory node by modulating the splicing of key regulators active during cell division.
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 pharmacology 13:860898 PubMed35401227
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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