Anti-hnRNP A1 (citrulline R97) antibody [EPR20176] - BSA and Azide free
- RabMAb
- Recombinant
- What is this?
Be the first to review this product! Submit a review
|
(0 Publication)
Rabbit Recombinant Monoclonal hnRNP A1 citrulline R97 antibody. Carrier free. Suitable for IP, Dot, WB and reacts with Transfected cell line - Human, Synthetic peptide - Human, Recombinant fragment, Human samples.
View Alternative Names
HNRPA1, HNRNPA1, Heterogeneous nuclear ribonucleoprotein A1, hnRNP A1, Helix-destabilizing protein, Single-strand RNA-binding protein, hnRNP core protein A1
- IP
Supplier Data
Immunoprecipitation - Anti-hnRNP A1 (citrulline R97) antibody [EPR20176] - BSA and Azide free (AB271981)
hnRNP A1 (citrulline R97) was immunoprecipitated from 0.35 mg of HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) transfected with GFP tagged PADI4 and treated with 10 mM CaCl2 for 2 hours, then 10 μM Ionomycin for 2 hours whole cell lysate with ab208028 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab208028 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution.
Lane 1 : HEK-293T transfected with GFP tagged PADI4 and treated with 10 mM CaCl2 for 2 hours, then 10 μM Ionomycin for 2 hours whole cell lysate 10 μg (Input).
Lane 2 : ab208028 IP in HEK-293T transfected with GFP tagged PADI4 and treated with 10 mM CaCl2 for 2 hours, then 10 μM Ionomycin for 2 hours whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab208028 in HEK-293T transfected with GFP tagged PADI4 and treated with 10 mM CaCl2 for 2 hours, then 10 μM Ionomycin for 2 hours whole cell lysate.
Exposure time : 10 seconds.
Blocking and dilution buffer : 5% NFDM/TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab208028).
All lanes:
Immunoprecipitation - Anti-hnRNP A1 (citrulline R97) antibody [EPR20176] (<a href='/en-us/products/primary-antibodies/hnrnp-a1-citrulline-r97-antibody-epr20176-ab208028'>ab208028</a>)
Predicted band size: 38 kDa
true
- WB
Supplier Data
Western blot - Anti-hnRNP A1 (citrulline R97) antibody [EPR20176] - BSA and Azide free (AB271981)
Blocking/Dilution buffer : 5% NFDM/TBST.
According to Uniprot annotation, isoform A1-A (34kD) is twenty times more abundant than isoform A1-B (39kD). PADs (including PADI2 and PADI4) are the enzymes that hydrolyze arginine to form citrulline, and this catalytic reaction also needs Ca2+ and ionomycin. Please refer to PMID : 26360112.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab208028).
Lanes 1 - 2:
Western blot - Anti-hnRNP A1 (citrulline R97) antibody [EPR20176] (<a href='/en-us/products/primary-antibodies/hnrnp-a1-citrulline-r97-antibody-epr20176-ab208028'>ab208028</a>) at 1/5000 dilution
Lanes 3 - 4:
Western blot - Anti-hnRNP A1 (citrulline R97) antibody [EPR20176] (<a href='/en-us/products/primary-antibodies/hnrnp-a1-citrulline-r97-antibody-epr20176-ab208028'>ab208028</a>) at 1/1000 dilution
Lanes 1 and 3:
Empty vector (vector control) transfected HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen), whole cell lysate at 10 µg
Lane 2:
HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell lysate transfected with GFP-tagged PADI2 and treated with 10 mM CaCl2 for 2 hours, followed by 10 uM Ionomycin for 2 hours at 10 µg
Lane 4:
HEK-293T (human epithelial cell line from embryonic kidney tranformed with large T antigen) whole cell lysate transfected with GFP-tagged PADI4 and treated with 10 mM CaCl2 for 2 hours, followed by 10 uM Ionomycin for 2 hours at 10 µg
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 1/100000 dilution
Predicted band size: 38 kDa
Observed band size: 34 kDa
true
Exposure time: 4s
- Dot
Supplier Data
Dot Blot - Anti-hnRNP A1 (citrulline R97) antibody [EPR20176] - BSA and Azide free (AB271981)
Dot blot analysis of hnRNP A1 (citrulline R97) labeled with ab208028 at 1/1000 dilution.
Lane 1 : hnRNP A1 (citrulline R97) peptide.
Lane 2 : hnRNP A1 (citrulline R97) non-citrulline peptide.
Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution was used as secondary antibody.
Blocking and dilution buffer : 5% NFDM/TBST.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab208028).
Related conjugates and formulations (1)
-
Anti-hnRNP A1 (citrulline R97) antibody [EPR20176]
Reactivity data
Product details
ab271981 is the carrier-free version of ab208028.
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
HnRNP A1 is involved in RNA binding and splicing contributing to the formation of spliceosomes the complexes responsible for pre-mRNA splicing. The protein aids in alternative splicing influencing mRNA diversity and stability. hnRNP A1 interacts with other proteins in the hnRNP family remodeling ribonucleoprotein complexes and affecting their functions. These interactions ensure proper mRNA maturation impacting gene expression regulation within the cell.
Pathways
HnRNP A1 is integral to critical cellular mechanisms such as the regulation of mRNA transport and splicing. It influences the DNA damage response pathway by modulating gene expression required for cellular repair and stability. hnRNP A1 also cooperates with other RNA binding proteins like the splicing factors SR proteins to orchestrate the splicing machinery. These interactions are pivotal in maintaining cellular homeostasis and response to stress.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
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