Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free)
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal PCIF1 antibody. Carrier free. Suitable for WB, IHC-P, ICC/IF, Flow Cyt (Intra), IP and reacts with Human, Mouse samples.
View Alternative Names
C20orf67, CAPAM, PPP1R121, PCIF1, mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase, Cap-specific adenosine methyltransferase, Phosphorylated CTD-interacting factor 1, Protein phosphatase 1 regulatory subunit 121, hCAPAM, hPCIF1
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells labelling PCIF1 with ab300487 at 1/50 (9.4 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing nuclear staining in HeLa cell line is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5 ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized MCF7 (human breast adenocarcinoma epithelial cell) cells labelling PCIF1 with ab300487 at 1/50 (9.4 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing nuclear staining in MCF7 cell line is observed. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 2.5 ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.Flow cytometric analysis of MCF7 (human breast adenocarcinoma epithelial cell) cells labelling PCIF1 with ab300487 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Human testis tissue labeling PCIF1 with ab300487 at 1/200 (2.35 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on human testis. The section was incubated with ab300487 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used.Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.
PCIF1 was immunoprecipitated from 0.35 mg HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate 10 ug with ab300487 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300487 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate 10 ug
Lane 2 : ab300487 IP in HeLa whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300487 in HeLa whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 84 seconds
All lanes:
Immunoprecipitation - Anti-PCIF1 antibody [EPR24319-207] (<a href='/en-us/products/primary-antibodies/pcif1-antibody-epr24319-207-ab300487'>ab300487</a>) at 1/1000 dilution
All lanes:
HeLa whole cell lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 84s
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.Flow cytometric analysis of NIH/3T3 (mouse embryonic fibroblast) cells labelling PCIF1 with ab300487 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling PCIF1 with ab300487 at 1/200 (2.35 ug/ml) followed by a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used. Nuclear staining on mouse liver. The section was incubated with ab300487 for 30 mins at room temperature.The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond Polymer Refine Detection) was used.Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labelling PCIF1 with ab300487 at 1/50 (9.4 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing nuclear staining in NIH/3T3 cell line is observed. was used to counterstain tubulin at 1/200 2.5 dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation.
PCIF1 was immunoprecipitated from 0.35 mg NIH/3T3 (mouse embryonic fibroblast), whole cell lysate 10 ug with ab300487 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300487 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : NIH/3T3 (mouse embryonic fibroblast), whole cell lysate 10 ug
Lane 2 : ab300487 IP in NIH/3T3 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300487 in NIH/3T3 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 minutes
This blot was developed using a high sensitivity ECL substrate.
Lanes 1 - 3:
Immunoprecipitation - Anti-PCIF1 antibody [EPR24319-207] (<a href='/en-us/products/primary-antibodies/pcif1-antibody-epr24319-207-ab300487'>ab300487</a>) at 1/1000 dilution
Lanes 1 - 3:
Immunoprecipitation - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (ab300488)
All lanes:
NIH/3T3 whole cell lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation. Blocking Buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-PCIF1 antibody [EPR24319-207] (<a href='/en-us/products/primary-antibodies/pcif1-antibody-epr24319-207-ab300487'>ab300487</a>) at 1/1000 dilution
Lane 1:
Jurkat (human T cell leukemia T lymphocyte), whole cell lysate
Lane 2:
293T (human embryonic kidney epithelial cell), whole cell lysate
Lane 3:
MCF7 (human breast adenocarcinoma epithelial cell), whole cell lysate
Lane 4:
NIH/3T3 (mouse embryonic fibroblast), whole cell lysate
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: 85 kDa
false
- WB
Supplier Data
Western blot - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation. Blocking Buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-PCIF1 antibody [EPR24319-207] (<a href='/en-us/products/primary-antibodies/pcif1-antibody-epr24319-207-ab300487'>ab300487</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervical adenocarcinoma epithelial cell) transfected with scrambled siRNA control, whole cell lysate
Lane 2:
HeLa transfected with siRNA specifically targeti PCIF1, whole cell lysate 40
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: 85 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-PCIF1 antibody [EPR24319-207] (BSA and Azide free) (AB300488)
This data was developed using ab300487, the same antibody clone in a different buffer formulation. Blocking Buffer and concentration : 5% NFDM/TBST
All lanes:
Western blot - Anti-PCIF1 antibody [EPR24319-207] (<a href='/en-us/products/primary-antibodies/pcif1-antibody-epr24319-207-ab300487'>ab300487</a>) at 1/1000 dilution
Lane 1:
Human testis tissue lysate
Lane 2:
Mouse testis tissue lysate
Lane 3:
Mouse liver tissue lysate
Lane 4:
Mouse heart tissue lysate
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 85 kDa
false
Exposure time: 3min
Related conjugates and formulations (1)
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Anti-PCIF1 antibody [EPR24319-207]
Reactivity data
Product details
ab300488 is a carrier free version of ab300487.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
PCIF1 modifies RNA molecules influencing mRNA cap structure formation and methylation. This activity is a part of the cap-binding complex which ensures proper RNA maturation and function. By interacting with the cap structure it plays a non-ignorable role in the control of RNA export translation and degradation facilitating the precise regulation of genetic information flow within cells. Its presence in the methyltransferase complex highlights its importance in cell biology.
Pathways
PCIF1 plays a prominent role in the mRNA capping and processing pathways. It partners with proteins such as RNA polymerase II in the pathway to ensure successful transcription and subsequent RNA modifications. The involvement in the mRNA cap methylation pathway highlights its connection with transcription and subsequent mRNA fate marking it as an important regulator in post-transcriptional gene expression regulation.
Product protocols
- Visit the General protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com