Rabbit Recombinant Monoclonal SNAPC1 antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra) and reacts with Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
WB | ICC/IF | Flow Cyt (Intra) | |
---|---|---|---|
Human | Tested | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/5000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/250 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/60 | Notes ab172730 - Rabbit monoclonal IgG, is suitable for use as an isotype control with this antibody. |
Part of the SNAPc complex required for the transcription of both RNA polymerase II and III small-nuclear RNA genes. Binds to the proximal sequence element (PSE), a non-TATA-box basal promoter element common to these 2 types of genes. Recruits TBP and BRF2 to the U6 snRNA TATA box.
SNAP43, SNAPC1, snRNA-activating protein complex subunit 1, SNAPc subunit 1, Proximal sequence element-binding transcription factor subunit gamma, Small nuclear RNA-activating complex polypeptide 1, snRNA-activating protein complex 43 kDa subunit, PSE-binding factor subunit gamma, PTF subunit gamma, SNAPc 43 kDa subunit
Rabbit Recombinant Monoclonal SNAPC1 antibody. Suitable for WB, ICC/IF, Flow Cyt (Intra) and reacts with Human samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
SNAPC1 also known as small nuclear RNA activating complex polypeptide 1 is a component of the snRNA-activating protein complex. It has a mass of about 43 kDa. SNAPC1 plays an important role in the transcription initiation of small nuclear RNA (snRNA) genes. It functions through interaction with other components of the SNAPc complex. Researchers observe its expression in various tissues but it appears particularly active in cells with high transcriptional demand.
The role of SNAPC1 lies in the assembly and regulation of the SNAPc complex. This complex functions primarily in the transcription of snRNA essential for mRNA processing and gene expression regulation. By participating in the formation of the snRNA-activating protein complex SNAPC1 facilitates the correct transcription and processing of snRNA a critical component in the spliceosomal machinery. It achieves this by forming stable interactions with other SNAPc components including SNAPC2 and SNAPC3 contributing to pre-mRNA splicing.
SNAPC1 integrates into two major cellular pathways: transcription initiation and RNA splicing. It closely interacts with elements such as RNA polymerase II and SNAPC4 within these pathways. By securing a stable interaction with these elements SNAPC1 supports efficient transcription of snRNA and its subsequent processing. The proper function of SNAPC1 and related proteins ensures the accuracy of mRNA splicing impacting overall gene expression and cellular function.
Defects or dysregulations involving SNAPC1 can link to disorders like Spinal Muscular Atrophy (SMA) and systemic lupus erythematosus (SLE). In SMA disruptions in snRNA processing lead to defects in the creation of essential proteins needed for motor neuron survival wherein SNAPC1 may hold a supporting role. In SLE abnormal snRNA processing can contribute to the production of autoantibodies linking SNAPC1 to the autoimmune pathway. SNAPC1's functional interactions with proteins like SMN (Survival of Motor Neuron) protein in SMA further illustrate its involvement in these disorders.
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We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Blocking/Dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-SNAPC1 antibody [EPR16466] (ab197015) at 1/5000 dilution
Lane 1: Human testis tissue lysate at 20 µg
Lane 2: HeLa (Human epithelial cells from cervix adenocarcinoma) cell lysate at 20 µg
All lanes: Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 43 kDa
Observed band size: 43 kDa
Blocking/Dilution buffer: 5% NFDM/TBST.
All lanes: Western blot - Anti-SNAPC1 antibody [EPR16466] (ab197015) at 1/5000 dilution
All lanes: Human fetal brain tissue lysate at 10 µg
All lanes: Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 43 kDa
Observed band size: 43 kDa
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa cells (Human epithelial cells from cervix adenocarcinoma) labeling SNAPC1 with ab197015 at 1/250 dilution, followed by Alexa Fluor®488 Goat Anti-Rabbit IgG H&L (Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077) secondary antibody at 1/500 dilution (green). Nuclear staining on HeLa cell line is observed. The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows:
-ve control 1: ab197015 at 1/250 dilution followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2: Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
Intracellular flow cytometric analysis ofU-87 MG (Human glioblastoma-astrocytoma epithelial cell line)cells labeling SNAPC1with ab197015 at 1/60 dilution (red)compared with a rabbit monoclonal IgG isotype control (black) and an unlabelled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (FITC) at 1/150 dilution was used as the secondary antibody.
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