Anti-hnRNP C1/C2 antibody [9G1]
- BOND RX™ Validated
- Recombinant
- What is this?
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(1 Publication)
Rabbit Recombinant Monoclonal hnRNP C1 + C2/HNRNPC antibody. Suitable for WB, IHC-P, ICC/IF, IP, Flow Cyt (Intra) and reacts with Human samples. Cited in 1 publication.
View Alternative Names
HNRPC, HNRNPC, Heterogeneous nuclear ribonucleoproteins C1/C2, hnRNP C1/C2
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-hnRNP C1/C2 antibody [9G1] (AB314004)
Overlay Peak curve showing MCF7 cells stained with ab314004 (red line) at 1/50. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100. T
hen 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*106cells) for 45min at 4°C. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG(H+L) at 1/200 dilution for 35min at 4°C.
Control antibody (green line) was Rabbit IgG (1ug/1*106cells) used under the same conditions. Acquisition of >10,000 events was performed.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP C1/C2 antibody [9G1] (AB314004)
IHC image of ab314004 diluted at 1/300 and staining in paraffin-embedded human breast cancer performed on a Leica Bond™ system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB. Secondary antibody only control : uses 1% BSA instead of primary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP C1/C2 antibody [9G1] (AB314004)
IHC image of ab314004 diluted at 1/300 and staining in paraffin-embedded human kidney tissue performed on a Leica Bond™ system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB. Secondary antibody only control : uses 1% BSA instead of primary antibody
- IP
Supplier Data
Immunoprecipitation - Anti-hnRNP C1/C2 antibody [9G1] (AB314004)
Immunoprecipitating HNRNPC in Hela whole cell lysate
Lane 1 : Rabbit control IgG instead of ab314004 in Hela whole cell lysate
Lane 2 : ab314004(3µg)+ Hela whole cell lysate(500µg)
Lane 3 : Hela whole cell lysate(20µg)
For western blotting, Goat polyclonal to rabbit IgG antibody was used as the secondary antibody (1/50000)
All lanes:
Immunoprecipitation - Anti-hnRNP C1/C2 antibody [9G1] (ab314004)
Lane 1:
Rabbit control IgG instead of ab314004 in Hela whole cell lysate
Lane 2:
ab314004 (3ug) and Hela whole cell lysate (500ug)
Lane 3:
Hela whole cell lysate at 20 µg
Secondary
All lanes:
Goat polyclonal to rabbit IgG antibody was used as the secondary antibody at 1/50000 dilution
false
- WB
Supplier Data
Western blot - Anti-hnRNP C1/C2 antibody [9G1] (AB314004)
All lanes:
Western blot - Anti-hnRNP C1/C2 antibody [9G1] (ab314004) at 1/1000 dilution
Lane 1:
HeLa cells
Lane 2:
293 cells
Lane 3:
Jurkat cells
Lane 4:
Raji cells
Lane 5:
MCF7 cells
Secondary
All lanes:
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 28 kDa,33 kDa,34 kDa,36 kDa
Observed band size: 42 kDa
false
Reactivity data
Product details
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
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
HnRNP C1/C2 participates in the assembly of large ribonucleoprotein complexes that are essential for mRNA metabolism. It acts as a core component of the spliceosome machinery where it influences the alternative splicing of pre-mRNA. Apart from its structural role hnRNP C1/C2 may contribute to the proper assembly and functioning of splicing factors and other proteins such as 4f4 within the nucleus suggesting its important role in gene expression regulation.
Pathways
HnRNP C1/C2 is involved in the RNA processing pathway directly impacting mRNA export and stability. By interacting with other proteins such as serine/arginine-rich splicing factors it modulates the splicing accuracy and efficiency of various transcripts. This participation in the spliceosome pathway emphasizes its importance in ensuring efficient gene expression and processing. hnRNP C1/C2 might also interact with various transcription machinery components linking RNA processing to transcriptional regulation.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Frontiers in immunology 16:1612935 PubMed40977716
2025
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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