Anti-MRPL48 抗体 [EPR16328] - BSA and Azide free
Anti-MRPL48 antibody [EPR16328] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal MRPL48 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra), IHC-P and reacts with Human, Mouse, Rat samples. Cited in 1 publication.
別名を表示する
CGI-118, HSPC290, MRPL48, Large ribosomal subunit protein mL48, L48mt, MRP-L48
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MRPL48 antibody [EPR16328] - BSA and Azide free (AB251194)
This data was developed using ab194826, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cervix carcinoma tissue labeling MRPL48 with ab194826 at 1/150 dilution. A Goat Anti-Rabbit IgG H&L (HRP) at 1/500 dilution was used as secondary (ab97051). Counterstain : Hematoxylin.
Inset image : negative control obtained using PBS instead of ab194826. Cytoplasm staining on human cervix carcinoma tissue was observed.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-MRPL48 antibody [EPR16328] - BSA and Azide free (AB251194)
This data was developed using ab194826, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of A431 cells labeling MRPL48 with ab194826 at 1/50 dilution. A Goat anti rabbit IgG (Alexa Fluor488) at 1/400 dilution (ab150077) was used as secondary antibody. Cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% triton X-100. Counterstain : DAPI. Cytoplasm staining on HepG2 cell line was observed.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-MRPL48 antibody [EPR16328] - BSA and Azide free (AB251194)
This data was developed using ab194826, the same antibody clone in a different buffer formulation.
Intracellular Flow Cytometry analysis of HeLa cells labelling MRPL48 (red) with purified ab194826 at dilution of 1/60. The secondary antibody used was Alexa Fluor® 488 goat-anti-rabbit IgG (1/2000). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. Isotype control antibody was Rabbit monoclonal IgG (black). The blue line shows cells without incubation with primary antibody and secondary antibody.
- IP
Supplier Data
Immunoprecipitation - Anti-MRPL48 antibody [EPR16328] - BSA and Azide free (AB251194)
This data was developed using ab194826, the same antibody clone in a different buffer formulation.
Western blot analysis of immunoprecipitation pellet from HepG2 cell lysate immunoprecipitated using ab194826 at 1/30 dilution (lane 1) or PBS control (lane 2)
For Western blot : ab194826 was used at 1/1000 dilution (0.6μg/ml). Secondary : Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1500 dilution.
All lanes:
Immunoprecipitation - Anti-MRPL48 antibody [EPR16328] (<a href='/products/primary-antibodies/mrpl48-antibody-epr16328-ab194826'>ab194826</a>)
Predicted band size: 24 kDa
false
- WB
Supplier Data
Western blot - Anti-MRPL48 antibody [EPR16328] - BSA and Azide free (AB251194)
This data was developed using ab194826, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-MRPL48 antibody [EPR16328] (<a href='/products/primary-antibodies/mrpl48-antibody-epr16328-ab194826'>ab194826</a>) at 1/10000 dilution
Lane 1:
HepG2 cell lysate at 20 µg
Lane 2:
HeLa cell lysate at 20 µg
Lane 3:
Jurkat cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 24 kDa
false
- WB
Supplier Data
Western blot - Anti-MRPL48 antibody [EPR16328] - BSA and Azide free (AB251194)
This data was developed using ab194826, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-MRPL48 antibody [EPR16328] (<a href='/products/primary-antibodies/mrpl48-antibody-epr16328-ab194826'>ab194826</a>) at 1/2000 dilution
All lanes:
Human fetal heart tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 24 kDa
false
- WB
Supplier Data
Western blot - Anti-MRPL48 antibody [EPR16328] - BSA and Azide free (AB251194)
This data was developed using ab194826, the same antibody clone in a different buffer formulation.
All lanes:
Western blot - Anti-MRPL48 antibody [EPR16328] (<a href='/products/primary-antibodies/mrpl48-antibody-epr16328-ab194826'>ab194826</a>) at 1/2000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Mouse heart lysate at 10 µg
Lane 3:
Rat brain lysate at 10 µg
Lane 4:
Rat heart lysate at 10 µg
Lane 5:
PC12 cell lysate at 10 µg
Lane 6:
NIH 3T3 cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 24 kDa
false
関連する標識済み抗体及び組成の異なる製品 (1)
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Anti-MRPL48 antibody [EPR16328]
Reactivity data
製品の詳細
ab251194 is the carrier-free version of ab194826.
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.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存温度
長期保存温度
保管に関する情報
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
MRPL48 contributes to the formation and function of the mitochondrial ribosome which is responsible for synthesizing proteins that are essential for mitochondrial respiration and energy production. This protein is part of the large subunit of the mitochondrial ribosome which includes many other mitochondrial ribosomal proteins. Together they form a complex responsible for translating mitochondrial mRNA into functional proteins.
Pathways
MRPL48 is actively engaged in mitochondrial translation a critical pathway for maintaining mitochondrial function and energy production. In this pathway it associates with other mitochondrial ribosomal proteins to produce enzymes necessary for the electron transport chain and ATP synthesis. MRPL48 also relates to oxidative phosphorylation where it plays a part in generating cellular energy linking it to proteins such as cytochrome c oxidase subunit IV.
製品プロトコール
- Visit the General protocols
- Visit the Troubleshooting
ターゲットの情報
文献 (1)
Recent publications for all applications. Explore the full list and refine your search
International journal of medical sciences 20:1079-1090 PubMed37484809
2023
Applications
Unspecified application
Species
Unspecified reactive species
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