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Anti-GTA MCP | Gene Transfer Agent (GTA) major capsid protein (MCP)
AS08 365 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Rhodobacterales
- Product Info
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Immunogen: KLH-conjugated conserved peptide sequence found in the Gene Transfer Agent (GTA) major capsid protein (MCP) encoded in Bacteria within the Rhodobacterales order of the class alpha-Proteobacteria including Rhodobacter sphaeroides UniProt: Q3J3K4
Host: Rabbit Clonality: Polyclonal Purity: Serum Format: Lyophilized Quantity: 100 µl Reconstitution: For reconstitution add 100 µl of sterile distilled water Storage: Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube. Tested applications: Western blot (WB) Recommended dilution: 1 : 1000 (WB) Expected | apparent MW: 31.4 | 32 kDa (predicted mature capsid protein of Rhodobacter capsulatus)
- Reactivity
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Confirmed reactivity: Dinoroseobacter shibae, Rhodobacter capsulatus, Ruegeria pomeroyi DSS-3 Predicted reactivity: Rhodobacterales
Species of your interest not listed? Contact usNot reactive in: No confirmed exceptions from predicted reactivity are currently known - Application Examples
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Application example
Roseobacter capsulatus cells, pelleted by centrifugation and resuspended in an equial volume of TE buffer and supernatant sample* were separated on 10% SDS-PAGE and blotted 1h to nitrocellulose. The "+" indicated R. capsulatus SB1003 (GTA positive) and "-" indicated R. capsulatus A1 (GTA capsid protein negative). Blots were blocked in 5% skim milk in TBST followed by incubation with anti-GTA antibodies (AS08 365) at dilution 1: 1000 at 4°C over night. After washes blots were incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Santa Cruz Biotechnology, Santa Cruz, CA) and specific bands were detected with chemiluminescence detection reagent.Exposure time was 30 seconds with CCD camera.
* - supernatant sample was obtained in a following way: cells were removed by two rounds of centrifugation at 17,000 g for 2 min. with sub-sample of the supernatant removed to a new tube. Two volumes of the cells or final culture supernatant were mixed with 1 volume of 3X SDS-PAGE sample buuffer (NEB).
- Additional Information
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Additional information: This product can be sold containing ProClin if requested - Background
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Background: Gene Transfer Agents (GTAs) are bacteriophage-like particles which function as a means to package and transfer genomic DNA between bacterial cells.GTA-mediated gene transfer might be an important phenomenon in natural microbial communities.
- Product Citations
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Selected references: Shimizu et al. (2022) Persulfide-Responsive Transcription Factor SqrR Regulates Gene Transfer and Biofilm Formation via the Metabolic Modulation of Cyclic di-GMP in Rhodobacter capsulatus, Microorganisms 10, no. 5: 908. https://doi.org/10.3390/microorganisms10050908
Koppenhofer et al. (2019). Integrated Transcriptional Regulatory Network of Quorum Sensing, Replication Control, and SOS Response in Dinoroseobacter shibae. Front. Microbiol., 12 April 2019 | https://doi.org/10.3389/fmicb.2019.00803.
Tomasch et al. (2018). Packaging of Dinoroseobacter shibae DNA into Gene Transfer Agent Particles Is Not Random. Genome Biol Evol. 2018 Jan 1;10(1):359-369. doi: 10.1093/gbe/evy005.
Mercer and Lang (2014). Identification of a predicted partner-switching system that affects production of the gene transfer agent RcGTA and stationary phase viability in Rhodobacter capsulatus. BMC Microbiol. 2014 Mar 19;14(1):71. - Protocols
- Antibody protocols
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