Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal hnRNP H antibody. Carrier free. Suitable for IHC-P, ICC/IF, IP, WB, Flow Cyt (Intra) and reacts with Mouse, Rat, Human, Recombinant fragment - Human samples.
View Alternative Names
HNRPH, HNRPH1, HNRNPH1, Heterogeneous nuclear ribonucleoprotein H, hnRNP H
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human prostatic hype tissue labelling hnRNP H with ab289974 at 1/500 dilution followed by LeicaDS9800 (Bond™, Polymer Refine Detection). Positive staining on human prostatic hyperplasia. The section was incubated with ab289974 for 30 mins at room temperatureThe immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is LeicaDS9800 (Bond™, Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized HeLa cells labeling hnRNP H with ab289974 at 1/100 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green). Confocal image showing nuclear staining in HeLa cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 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 dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human testis tissue labelling hnRNP H with ab289974 at 1/500 dilution followed by LeicaDS9800 (Bond™, Polymer Refine Detection). Positive staining on human testis. The section was incubated with ab289974 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 LeicaDS9800 (Bond™, Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Intracellular flow analysis of 4% paraformaldehyde fixed, 90% methanol permeabilized HeLa (Human cervix adenocarcinoma epithelial cell) cells labelling hnRNP H with ab289974 at 1/500 dilution (0.1μg) (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). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat testis tissue labelling hnRNP H with ab289974 at 1/500 dilution followed by LeicaDS9800 (Bond™, Polymer Refine Detection). Positive staining on rat testis. The section was incubated with ab289974 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 LeicaDS9800 (Bond™, Polymer Refine Detection).
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized C2C12 cells llabeling hnRNP H with ab289974 at 1/100 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed secondary antibody at 1/1000 dilution (Green). Confocal image showing nuclear staining in C2C12 cell line. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed, 90% methanol permeabilized C2C12 (Mouse myoblasts myoblast) cells labelling hnRNP H with ab289974 at 1/500 dilution (0.1μg) (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). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse testis tissue labelling hnRNP H with ab289974 at 1/500 dilution followed by LeicaDS9800 (Bond™, Polymer Refine Detection). Positive staining on mouse testis. The section was incubated with ab289974 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 LeicaDS9800 (Bond™, Polymer Refine Detection) .
Heat mediated antigen retrieval with Citrate buffer (pH 6.0, epitope retrieval solution 1) for 20 mins
- IP
Lab
Immunoprecipitation - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
hnRNP H was immunoprecipitated from HeLa (human epithelial cell line from cervix adenocarcinoma), whole cell lysate with ab289974 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab289974 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (human epithelial cell line from cervix adenocarcinoma), whole cell lysate 10 μg
Lane 2 : ab289974 IP in HeLa whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab289974 in HeLa whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 seconds
All lanes:
Immunoprecipitation - Anti-hnRNP H antibody [EPR25302-12] (<a href='/en-us/products/primary-antibodies/hnrnp-h-antibody-epr25302-12-ab289974'>ab289974</a>)
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
- IP
Lab
Immunoprecipitation - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
hnRNP H was immunoprecipitated from C2C12 (Mouse myoblasts myoblast), whole cell lysate with ab289974 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab289974 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : C2C12 (Mouse myoblasts myoblast), whole cell lysate 10 μg
Lane 2 : ab289974 IP in C2C12 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab289974 in C2C12 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 5.5 seconds
All lanes:
Immunoprecipitation - Anti-hnRNP H antibody [EPR25302-12] (<a href='/en-us/products/primary-antibodies/hnrnp-h-antibody-epr25302-12-ab289974'>ab289974</a>)
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
- WB
Lab
Western blot - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 23667175, PMID : 21915099)
Exposure times : Lane 1 : 3 minutes Lane 2-6 : 15 seconds
All lanes:
Western blot - Anti-hnRNP H antibody [EPR25302-12] (<a href='/en-us/products/primary-antibodies/hnrnp-h-antibody-epr25302-12-ab289974'>ab289974</a>) at 1/1000 dilution
Lane 1:
Human testis tissue lysate at 20 µg
Lane 2:
Mouse colon tissue lysate at 20 µg
Lane 3:
Mouse liver tissue lysate at 20 µg
Lane 4:
Mouse testis tissue lysate at 20 µg
Lane 5:
Rat liver tissue lysate at 20 µg
Lane 6:
Rat testis tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
- WB
Lab
Western blot - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 23667175, PMID : 21915099)
Exposure times : Lane 1-3 : 3 seconds Lane 4-6 : 5 seconds
All lanes:
Western blot - Anti-hnRNP H antibody [EPR25302-12] (<a href='/en-us/products/primary-antibodies/hnrnp-h-antibody-epr25302-12-ab289974'>ab289974</a>) at 1/1000 dilution
Lane 1:
HEK-293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 2:
U-2OS(human bone osteosarcoma epithelial cell), whole cell lysate at 20 µg
Lane 3:
MOLT-4 (human lymphoblastic leukemia T lymphoblast), whole cell lysate at 20 µg
Lane 4:
C2C12 (Mouse myoblasts myoblast), whole cell lysate at 20 µg
Lane 5:
NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 20 µg
Lane 6:
C6 (rat glial tumor glial cell), whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa
false
- WB
Lab
Western blot - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 23667175, PMID : 21915099)
Exposure time : 8 seconds
All lanes:
Western blot - Anti-hnRNP H antibody [EPR25302-12] (<a href='/en-us/products/primary-antibodies/hnrnp-h-antibody-epr25302-12-ab289974'>ab289974</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
HeLa transfected with siRNA specifically targeti hnRNP H 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: 49 kDa
Observed band size: 50 kDa
false
- WB
Lab
Western blot - Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free (AB289999)
This data was developed using ab289974, the same antibody clone in a different buffer formulation.
This antibody reacts with HNRPH1 and HNRPH2, but does not react with HNRNPF and HNRPH3.
Exposure time : 114 seconds
All lanes:
Western blot - Anti-hnRNP H antibody [EPR25302-12] (<a href='/en-us/products/primary-antibodies/hnrnp-h-antibody-epr25302-12-ab289974'>ab289974</a>) at 1/1000 dilution
Lane 1:
Myc-tagged human HNRPH1 (HNRNPH1) (NM_005520) recombinant protein (20 ng)
Lane 2:
Myc-tagged human HNRPH2 (HNRNPH2) (NM_019597) recombinant protein (20 ng)
Lane 3:
Myc-tagged human hnRNP F (HNRNPF) (NM_001098207) recombinant protein(20 ng)
Lane 4:
Myc-tagged human HNRPH3 (HNRNPH3) (NM_021644) recombinant protein (20 ng)
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: 49 kDa
Observed band size: 50 kDa
false
Reactivity data
Product details
ab289999 is the carrier-free version of ab289974.
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
HnRNP H acts as a splicing regulator and is a member of the hnRNP complex. It binds to the RNA cis-elements influencing alternative splicing events. hnRNP H can interact with other RNA-binding proteins and regulatory elements to modulate the inclusion or exclusion of certain exons. This helps in generating different mRNA variants allowing the production of protein diversity from a single gene.
Pathways
HnRNP H participates in the alternative splicing and mRNA processing pathways. The proteins it interacts with such as serine/arginine-rich splicing factor 1 (SRSF1) help facilitate the splicing mechanisms. hnRNP H's ability to influence splicing makes it essential for cellular processes like development and differentiation by producing proteins with varied functionalities.
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