Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175]
- RabMAb
- Recombinant
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(2 Publications)
Rabbit Recombinant Monoclonal hnRNP A1 citrulline R88 + R92 antibody. Suitable for IP, Dot, WB, Flow Cyt (Intra) and reacts with Human, Synthetic peptide samples. Cited in 2 publications.
View Alternative Names
HNRPA1, HNRNPA1, Heterogeneous nuclear ribonucleoprotein A1, hnRNP A1, Helix-destabilizing protein, Single-strand RNA-binding protein, hnRNP core protein A1
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175] (AB208027)
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) cells transfected with PADI4 expression vector, then treated with 10 mM CaCl2 and 10 μM Ionomycin for 2 hours, labeling hnRNP A1 with ab208027 at 1/5000 dilution (right panel) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (left panel). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 647) (ab150079) at 1/2000 dilution was used as the secondary antibody.
The CaCl2 and Ionomycin treated GFP positive cell population gives a positive signal. (Right panel, Q2).
- IP
Supplier Data
Immunoprecipitation - Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175] (AB208027)
hnRNP A1 was immunoprecipitated from 0.35 mg HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) with ab208027 at 1/30 dilution, whole cell lysate. Western blot was performed from the immunoprecipitate using ab208027 at 1/10000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution.
Lane 1 : HEK-293T transfected with PADI4 expression vector, then treated with 10 mM CaCl2 and 10μM Ionomycin for 2 hours whole cell lysate 10 μg (Input).
Lane 2 : ab208027 IP in HEK-293T transfected with PADI4 expression vector, then treated with 10 mM CaCl2 and 10 μM Ionomycin for 2 hours whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab208027 in HEK-293T transfected with PADI4 expression vector, then treated with 10 mM CaCl2 and 10 μM Ionomycin for 2 hours whole cell lysate.
Blocking/Dilution buffer : 5% NFDM/TBST.
Exposure time : 1 second.
All lanes:
Immunoprecipitation - Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175] (ab208027)
Predicted band size: 38 kDa
Observed band size: 31 kDa,34 kDa,37 kDa
false
- WB
Supplier Data
Western blot - Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175] (AB208027)
hnRNP A1(Uniprot P09651), isoform A1-A (34kD) is twenty times more abundant than isoform A1-B (39kD). The molecular weights of hnRNP A1L2 (Q32P51), hnRNP A0 (Q13151) and hnRNP A2B1 (P22626) are 34kD, 31kD and 37kD respectively.
PAD enzymes (including PADI2 and PADI4) hydrolyze arginine to form citrulline, Ca2+ and ionomycin are also required for this catalytic reaction (PMID : 26360112).
Blocking/Dilution buffer : 5% NFDM/TBST
Exposure times : Lane 1-2 : 1 second; Lane 3-4 : 2 seconds.
All lanes:
Western blot - Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175] (ab208027) at 1/5000 dilution
Lane 1:
HEK-293T (human epithelial cell line from embryonic kidney transformed with large T antigen) transfected with empty vector (control) then treated with 10 mM CaCl2 and 10 μM Ionomycin for 2 hours, whole cell lysate at 20 µg
Lane 2:
HEK-293T transfected with a PADI4 expression vector then treated with 10 mM CaCl2 and 10 μM Ionomycin for 2 hours, whole cell lysate at 20 µg
Lane 3:
HEK-293T transfected with an empty vector (control) then treated with 10 mM CaCl2 and 10 μM Ionomycin for 2 hours, whole cell lysate at 20 µg
Lane 4:
HEK-293T transfected with a PADI2 expression vector then treated with 10 mM CaCl2 and 10 μM Ionomycin for 2 hours, whole cell lysate at 20 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: 31 kDa,37 kDa,39 kDa
true
- Dot
Supplier Data
Dot Blot - Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175] (AB208027)
Dot Blot analysis of hnRNP A1 (citrulline R88 + R92) labeled with ab208027 at 1/1000 dilution.
Lane 1 : hnRNP A1 (citrulline R88/92) peptide.
Lane 2 : hnRNP A3 (citrulline R109/113) peptide.
Lane 3 : hnRNP A0 (citrulline R81/85) peptide.
Lane 4 : hnRNP A2B1 (citrulline R95/99) peptide.
Lane 5 : CCDC51 (citrulline R142) peptide.
Lane 6 : hnRNP A1 non-citrulline peptide.
Lane 7 : hnRNP A1 (citrulline R88) peptide.
Lane 8 : hnRNP A1 (citrulline R92) peptide.
Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution was used as secondary antibody.
Blocking/Dilution buffer : 5% NFDM/TBST.
Exposure time : 30 seconds.
Related conjugates and formulations (1)
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Anti-hnRNP A1 (citrulline R88 + R92) antibody [EPR20175] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
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Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
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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.
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Target data
Publications (2)
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Bladder cancer (Amsterdam, Netherlands) 9:29-40 PubMed38994477
2023
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Science advances 8:eabq7289 PubMed36563164
2022
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Product promise
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