Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- What is this?
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(2 Publications)
Rabbit Recombinant Monoclonal SMN/Gemin 1 antibody. Carrier free. Suitable for IHC-Fr, ICC/IF, WB and reacts with Human samples. Cited in 2 publications.
View Alternative Names
SMN, SMNT, SMN2, SMNC, SMN1, Survival motor neuron protein, Component of gems 1, Gemin-1
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
This data was developed using ab108531, the same antibody clone in a different buffer formulation.
Immunocytochemistry/Immunofluorescence analysis of SH-SY5Y cells labelling Gemin 1 with purified ab108531 at 1/250. Cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500) was used as the secondary antibody. DAPI (blue) was used as the nuclear counterstain. ab7291, a mouse anti-tubulin (1/500) and ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500) were also used.
Control 1 : primary antibody (1/100) and secondary antibody, ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500).
Control 2 : ab7291 (1/1000) and secondary antibody, ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500).
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
IHC image of SMN/Gemin 1 staining in a section of human normal frozen hippocampus* performed on a Leica Biosystems BOND® RX instrument using the standard protocol. The section was fixed in 10% paraformaldehyde (10 min) prior to staining. The section was incubated with ab108531, 2.5ugml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody. *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times. This data was developed using ab108531, the same antibody clone in a different buffer formulation.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
IHC image of SMN/Gemin 1 staining in a section of human normal frozen cervix* performed on a Leica Biosystems BOND® RX instrument using the standard protocol. The section was fixed in 10% paraformaldehyde (10 min) prior to staining. The section was incubated with ab108531, 1ugml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody. For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times. *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre This data was developed using ab108531, the same antibody clone in a different buffer formulation.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
IHC image of SMN/Gemin 1 staining in a section of human normal frozen prostate cancer* performed on a Leica Biosystems BOND® RX instrument using the standard protocol. The section was fixed in 10% paraformaldehyde (10 min) prior to staining. The section was incubated with ab108531, 1ugml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX. The inset secondary-only control image is taken from an identical assay without primary antibody. *Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times. This data was developed using ab108531, the same antibody clone in a different buffer formulation.
- WB
Unknown
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
This data was developed using ab108531, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] (<a href='/en-us/products/primary-antibodies/smn-gemin-1-antibody-epr4429-ab108531'>ab108531</a>) at 1/1000 dilution
Lane 1:
K562 cell lysate at 20 µg
Lane 2:
HEK-293 cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 32 kDa
Observed band size: 35 kDa
false
- WB
Unknown
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
This data was developed using ab108531, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] (<a href='/en-us/products/primary-antibodies/smn-gemin-1-antibody-epr4429-ab108531'>ab108531</a>) at 1/1000 dilution
All lanes:
HeLa cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 105 kDa,11 kDa,32 kDa
Observed band size: 105 kDa,14 kDa,35 kDa,50 kDa
false
- WB
Unknown
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
This data was developed using ab108531, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] (<a href='/en-us/products/primary-antibodies/smn-gemin-1-antibody-epr4429-ab108531'>ab108531</a>) at 1/5000 dilution
All lanes:
HepG2 cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 32 kDa
Observed band size: 35 kDa
false
- WB
Unknown
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
This data was developed using ab108531, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] (<a href='/en-us/products/primary-antibodies/smn-gemin-1-antibody-epr4429-ab108531'>ab108531</a>) at 1/1000 dilution
Lane 1:
HeLa cell lysate at 10 µg
Lane 2:
HepG2 cell lysate at 10 µg
Lane 3:
K562 cell lysate at 10 µg
Lane 4:
293T cell lysate at 10 µg
Secondary
All lanes:
HRP-conjugated goat anti-rabbit IgG at 1/2000 dilution
Predicted band size: 32 kDa
false
- WB
Lab
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] - BSA and Azide free (AB247685)
This data was developed using ab108531, the same antibody clone in a different buffer formulation.
Western blot : Rabbit Monoclonal [EPR4429] to SMN/Gemin 1 ab108531 staining at 1/1000 dilution, shown in green; Mouse anti alpha Tubulin (ab7291) loading control staining at 1/20,000 dilution, shown in magenta.
A band was observed at 32 kDa in Wild-type A549 cell lysates with no signal observed at this size in SMN1 knockout A549 cell line.
To generate this image, samples were run on an SDS-PAGE gel then transferred onto a nitrocellulose membrane. Membranes were blocked in 3pc Milk in TBS-0.1 % Tween® 20 (TBS-T) before incubation with primary antibodies overnight at 4 °C. Blots were washed four times in TBS-T, incubated with secondary antibodies for 1 h at room temperature, washed again four times then imaged.
Secondary antibodies used were Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20,000 dilution.
All lanes:
Western blot - Anti-SMN/Gemin 1 antibody [EPR4429] (<a href='/en-us/products/primary-antibodies/smn-gemin-1-antibody-epr4429-ab108531'>ab108531</a>) at 1/1000 dilution
Lane 1:
Wild-type A549 at 20 µg
Lane 2:
SMN1 knockout A549 at 20 µg
Lane 2:
Western blot - Human SMN1 knockout A549 cell line (<a href='/en-us/products/cell-lines/human-smn1-knockout-a549-cell-line-ab301247'>ab301247</a>) at 20 µg
Lane 3:
HeLa at 20 µg
Lane 4:
PC-3 at 20 µg
Secondary
All lanes:
Goat anti-Rabbit 800CW & Goat anti-Mouse 680RD at 1/20000 dilution
Predicted band size: 32 kDa
Observed band size: 32 kDa
false
Related conjugates and formulations (8)
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Anti-SMN/Gemin 1 antibody [EPR4429]
-
660 APC
APC Anti-SMN/Gemin 1 antibody [EPR4429]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-SMN/Gemin 1 antibody [EPR4429]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-SMN/Gemin 1 antibody [EPR4429]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-SMN/Gemin 1 antibody [EPR4429]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-SMN/Gemin 1 antibody [EPR4429]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-SMN/Gemin 1 antibody [EPR4429]
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578 PE
PE Anti-SMN/Gemin 1 antibody [EPR4429]
Reactivity data
Product details
ab247685 is the carrier-free version of ab108531.
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
The SMN protein operates within the SMN-Gemin complex a multi-protein assembly important for snRNP biogenesis and pre-mRNA splicing. This complex coordinates the maturation and transport of snRNPs facilitating the processing of precursor mRNAs in the nucleus. SMN and associated Gemin proteins mediate the assembly of Sm proteins onto snRNA ensuring accurate splicing mechanisms necessary for gene expression.
Pathways
The SMN protein is notably involved in the chaperone-assisted assembly pathway related to snRNP biogenesis. It plays a central role in the spliceosome assembly process working closely with Sm proteins and other RNA-binding proteins. Importantly SMN interacts with the ribonucleoprotein complex influencing mRNA splicing which integrates into the broader cell signaling pathways such as the cholinergic agonist pathways and RNA splicing pathways that regulate neuromuscular communication.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (2)
Recent publications for all applications. Explore the full list and refine your search
Advanced materials (Deerfield Beach, Fla.) 35:e2302801 PubMed37589156
2023
Applications
Unspecified application
Species
Unspecified reactive species
Oncology letters 26:409 PubMed37600337
2023
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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