Rabbit Recombinant Monoclonal HNRPH2/HNRNPH2 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB, ELISA and reacts with Human, Mouse, Rat samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
IHC-P | ICC/IF | WB | ELISA | |
---|---|---|---|---|
Human | Tested | Tested | Tested | Tested |
Mouse | Tested | Expected | Tested | Expected |
Rat | Tested | Expected | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Mouse | Dilution info - | Notes - |
Species Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
This protein is a component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes which provide the substrate for the processing events that pre-mRNAs undergo before becoming functional, translatable mRNAs in the cytoplasm. Binds poly(RG).
FTP3, HNRPH2, HNRNPH2, Heterogeneous nuclear ribonucleoprotein H2, hnRNP H2, FTP-3, Heterogeneous nuclear ribonucleoprotein H', hnRNP H'
Rabbit Recombinant Monoclonal HNRPH2/HNRNPH2 antibody. Carrier free. Suitable for IHC-P, ICC/IF, WB, ELISA and reacts with Human, Mouse, Rat samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
ab250397 is the carrier-free version of Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171.
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
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.
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.
HNRPH2 also known as hnRNP H2 is a member of the heterogeneous nuclear ribonucleoprotein (hnRNP) family. It assists in RNA binding and processing playing a role in pre-mRNA splicing and mRNA metabolism. HNRPH2 has a molecular mass of approximately 49 kDa. Researchers have identified its expression in various tissues with a notable presence in the nucleus where RNA processing occurs.
HNRPH2 participates in critical cellular mechanisms involving RNA. It plays a role in hnRNP complexes which help in the nuclear-cytoplasmic transport of mRNAs. This protein aids in alternative splicing which allows cells to produce multiple protein variants from a single gene. By binding to specific sequences on RNA HNRPH2 influences the maturation and stability of RNA molecules ensuring accurate gene expression.
HNRPH2 functions in the regulation of gene expression and RNA splicing pathways. It associates with the spliceosome which is essential in removing introns from pre-mRNA. This activity links it to processes like the alternative splicing pathway integral for creating protein diversity in cells. Interactions with other hnRNP proteins such as hnRNP A1 highlight its involvement in maintaining cellular RNA homeostasis.
Alterations in HNRPH2 are linked to neurological disorders and cancers. Mutations in the HNRPH2 gene have been associated with Bainbridge-Ropers syndrome a neurodevelopmental disorder suggesting the gene's role in neural development. Disruptions in its function may also relate to cancer where the abnormal splicing of mRNAs can promote tumorigenesis. HNRPH2's interaction with proteins such as TDP-43 implies its possible involvement in neurodegenerative diseases.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
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Terms & Conditions.
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Antigen: Human HNRNPH1, Human HNRNPH3, Human HNRNPF, Human HNRNPH2
Antigen Concentration: 1000 ng/ml
Primary antibody (Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171) concentration range: 1000-0 ng/ml
Secondary antibody: Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) (1:2500 dilution)
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded sections of rat stomach tissue staining HNRPH2/HNRNPH2 with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at 1/1000 dilution and ready to use secondary Goat Anti-Rabbit IgG H&L (HRP polymer) (Goat Anti-Rabbit IgG H&L (HRP polymer) ab214880). Counterstained with hematoxylin. Heat mediated antigen retrieval was done using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). The section was incubated with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at +4° C overnight. Nuclear staining on rat stomach.
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Immunocytochemical analysis of 0.1% TritonX-100 permeabilised 100% methanol fixed HEK-293 cells staining HNRPH2/HNRNPH2 with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at 1/100 dilution and secondary Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution. Counterstained with Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) at 1/200 dilution. Nuclear counterstain was DAPI. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). Confocal image showing nuclear staining in HEK-293 cell line.
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded sections of mouse stomach tissue staining HNRPH2/HNRNPH2 with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at 1/1000 dilution and ready to use secondary Goat Anti-Rabbit IgG H&L (HRP polymer) (Goat Anti-Rabbit IgG H&L (HRP polymer) ab214880). Counterstained with hematoxylin. Heat mediated antigen retrieval was done using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). The section was incubated with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at +4° C overnight. Nuclear staining on mouse stomach.
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 was shown to react with HNRNPH2 in wild-type DMS 53 cells in Western blot with loss of signal observed in a HNRNPH2 siRNA knockdown cell line. Cell lysates from wild-type DMS 53 transfected with either scrambled siRNA or HNRNPH2 siRNA were subjected to SDS-PAGE. Membranes were blocked in 5% milk in TBST for 1 hour before incubation with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 overnight at 4 °C at a 1/1000 dilution. Blots were incubated with secondary antibodies at 0.2 µg/mL before imaging.
This data was provided by YCharOS Inc., an open science company with the mission of characterizing commercially available antibody reagents for all human proteins. Abcam and YCharOS are working together to help address the reproducibility crisis by enabling the life science community to better evaluate commercially available antibodies.
All lanes: Western blot - Anti-HNRPH2/HNRNPH2 antibody [EPR12171] (Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171) at 1/1000 dilution
Lane 1: Wild-type DMS 53 transfected with scrambled siRNA control lysate at 40 µg
Lane 2: DMS 53 transfected with siRNA specifically targeting HNRNPH2 cell lysate at 40 µg
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin embedded sections of human endometrium tissue staining HNRPH2/HNRNPH2 with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at 1/1000 dilution and ready to use secondary Goat Anti-Rabbit IgG H&L (HRP polymer) (Goat Anti-Rabbit IgG H&L (HRP polymer) ab214880). Counterstained with hematoxylin. Heat mediated antigen retrieval was done using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). The section was incubated with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at +4° C overnight. Nuclear staining on human endometrium.
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer: 5% NFDM/TBST. The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 23667175, PMID: 21915099)
Lanes 1 - 9: Western blot - Anti-HNRPH2/HNRNPH2 antibody [EPR12171] (Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171) at 1/1000 dilution
Lanes 1 - 9: Western blot - Anti-HNRPH2/HNRNPH2 antibody [EPR12171] - BSA and Azide free (ab250397) at 1/1000 dilution
Lane 1: MCF7 (Human breast adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2: 293T (Human embryonic kidney epithelial cell)
Lane 3: Jurkat (Human T cell leukemia T lymphocyte) whole cell lysate
Lane 4: Mouse midbrain lysate
Lane 5: Mouse brain lysate
Lane 6: Mouse spleen lysate
Lane 7: C6 (Rat glial tumor glial cell) whole cell lysate
Lane 8: Rat brain lysate
Lane 9: Rat midbrain lysate
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Exposure time: 100s
This data was developed using Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of parafin embedded sections of human stomach tissue staining HNRPH2/HNRNPH2 with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at 1/1000 dilution and ready to use secondary Goat Anti-Rabbit IgG H&L (HRP polymer) (Goat Anti-Rabbit IgG H&L (HRP polymer) ab214880). Counterstained with hematoxylin. Heat mediated antigen retrieval was done using Antigen Retrieval Buffer (100X Tris-EDTA Buffer, pH 9.0) ab93684 (Tris/EDTA buffer, pH 9.0). The section was incubated with Anti-HNRPH2/HNRNPH2 antibody [EPR12171] ab181171 at +4° C overnight. Nuclear staining on human stomach.
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