Anti-hnRNP H 抗体 [EPR25302-12] - BSA and Azide free (ab289999)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR25302-12] to hnRNP H - BSA and Azide free
- Suitable for: ICC/IF, WB, IHC-P, Flow Cyt (Intra), IP
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
製品の概要
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製品名
Anti-hnRNP H antibody [EPR25302-12] - BSA and Azide free
hnRNP H 一次抗体 製品一覧 -
製品の詳細
Rabbit monoclonal [EPR25302-12] to hnRNP H - BSA and Azide free -
由来種
Rabbit -
アプリケーション
適用あり: ICC/IF, WB, IHC-P, Flow Cyt (Intra), IPmore details -
種交差性
交差種: Mouse, Rat, Human -
免疫原
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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ポジティブ・コントロール
- WB: HeLa, HEK-293T, U-2OS, MOLT-4, C2C12, NIH/3T3 and C6 whole cell lysates; Mouse testis, colon and liver tissue lysates; Rat liver and testis tissue lysates. IHC-P: Human testis and prostatic hyperplasia tissue; Mouse testis tissue; Rat testis tissue. ICC/IF: HeLa and C2C12 cells Flow Cyt (intra): HeLa and C2C12 cells. IP: HeLa and C2C12 whole cell lysates.
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特記事項
ab289999 is the carrier-free version of ab289974.
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.
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 production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
製品の特性
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製品の状態
Liquid -
保存方法
Shipped at 4°C. Store at +4°C. -
バッファー
pH: 7.20
Constituent: 100% PBS -
キャリア・フリー
はい -
Concentration information loading...
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精製度
Protein A purified -
ポリ/モノ
モノクローナル -
クローン名
EPR25302-12 -
アイソタイプ
IgG -
研究分野
関連製品
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Compatible Secondaries
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Isotype control
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Related Products
アプリケーション
The Abpromise guarantee
Abpromise保証は、 次のテスト済みアプリケーションにおけるab289999の使用に適用されます
アプリケーションノートには、推奨の開始希釈率がありますが、適切な希釈率につきましてはご検討ください。
アプリケーション | Abreviews | 特記事項 |
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ICC/IF |
Use at an assay dependent concentration.
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WB |
Use at an assay dependent concentration. Detects a band of approximately 50 kDa (predicted molecular weight: 49 kDa).
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IHC-P |
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
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Flow Cyt (Intra) |
Use at an assay dependent concentration.
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IP |
Use at an assay dependent concentration.
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特記事項 |
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ICC/IF
Use at an assay dependent concentration. |
WB
Use at an assay dependent concentration. Detects a band of approximately 50 kDa (predicted molecular weight: 49 kDa). |
IHC-P
Use at an assay dependent concentration. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Flow Cyt (Intra)
Use at an assay dependent concentration. |
IP
Use at an assay dependent concentration. |
ターゲット情報
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機能
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. Mediates pre-mRNA alternative splicing regulation. Inhibits, together with CUGBP1, insulin receptor (IR) pre-mRNA exon 11 inclusion in myoblast. Binds to the IR RNA. Binds poly(RG). -
組織特異性
Expressed ubiquitously. -
配列類似性
Contains 3 RRM (RNA recognition motif) domains. -
ドメイン
Each quasi-RRM repeat bound poly(RG), while only the N-terminal QRRM bound poly(RC) and poly(RU). None of the repeats bound detectable amounts of poly(RA). -
細胞内局在
Nucleus > nucleoplasm. - Information by UniProt
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参照データベース
- Entrez Gene: 3187 Human
- Entrez Gene: 59013 Mouse
- Entrez Gene: 140931 Rat
- Omim: 601035 Human
- SwissProt: P31943 Human
- SwissProt: O35737 Mouse
- SwissProt: Q8VHV7 Rat
- Unigene: 604001 Human
see all -
別名
- DKFZp686A15170 antibody
- Heterogeneous nuclear ribonucleoprotein H antibody
- Heterogeneous nuclear ribonucleoprotein H1 (H) antibody
see all
画像
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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
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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.
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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.
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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
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All lanes : Anti-hnRNP H antibody [EPR25302-12] (ab289974) at 1/1000 dilution
Lane 1 : Human testis tissue lysate
Lane 2 : Mouse colon tissue lysate
Lane 3 : Mouse liver tissue lysate
Lane 4 : Mouse testis tissue lysate
Lane 5 : Rat liver tissue lysate
Lane 6 : Rat testis tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/100000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa why is the actual band size different from the predicted?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
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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.
-
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.
-
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
-
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
-
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
-
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
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All lanes : Anti-hnRNP H antibody [EPR25302-12] (ab289974) 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 : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 49 kDa
Observed band size: 50 kDa why is the actual band size different from the predicted?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
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All lanes : Anti-hnRNP H antibody [EPR25302-12] (ab289974) at 1/1000 dilution
Lane 1 : HEK-293T (human embryonic kidney epithelial cell) whole cell lysate
Lane 2 : U-2OS(human bone osteosarcoma epithelial cell), whole cell lysate
Lane 3 : MOLT-4 (human lymphoblastic leukemia T lymphoblast), whole cell lysate
Lane 4 : C2C12 (Mouse myoblasts myoblast), whole cell lysate
Lane 5 : NIH/3T3 (mouse embryonic fibroblast), whole cell lysate
Lane 6 : C6 (rat glial tumor glial cell), whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/100000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa why is the actual band size different from the predicted?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
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All lanes : Anti-hnRNP H antibody [EPR25302-12] (ab289974) at 1/1000 dilution
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate
Lane 2 : HeLa transfected with siRNA specifically targeti hnRNP H whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution
Predicted band size: 49 kDa
Observed band size: 50 kDa why is the actual band size different from the predicted?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
プロトコール
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
データシートおよび資料
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Datasheet download
Certificate of Compliance
参考文献 (0)
ab289999 は論文での使用が確認できていません。