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Anti-hnRNP A1抗体[9H10] (ab5832)

Reviews (5)Q&A (2)References (52)
Western blot - Anti-hnRNP A1 antibody [9H10] (ab5832)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP A1 antibody [9H10] (ab5832)
  • Western blot - Anti-hnRNP A1 antibody [9H10] (ab5832)
  • Flow Cytometry - Anti-hnRNP A1 antibody [9H10] (ab5832)
  • Immunoprecipitation - Anti-hnRNP A1 antibody [9H10] (ab5832)

Key features and details

  • Mouse monoclonal [9H10] to hnRNP A1
  • Suitable for: Flow Cyt, IHC-P, ELISA, WB, IP, ICC/IF
  • Reacts with: Mouse, Human
  • Isotype: IgG2b

概述

  • 产品名称

    Anti-hnRNP A1抗体[9H10]
    参阅全部 hnRNP A1 一抗

  • 描述

    小鼠单克隆抗体[9H10] to hnRNP A1

  • 宿主

    Mouse

  • 经测试应用

    适用于: Flow Cyt, IHC-P, ELISA, WB, IP, ICC/IFmore details

  • 种属反应性

    与反应: Mouse, Human

  • 免疫原

    Full length hnRNPA1 native protein (partially purified) from HeLa cells (Human).

  • 常规说明

    The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.

    If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As

性能

  • 形式

    Liquid

  • 存放说明

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

  • 存储溶液

    Preservative: 0.1% Sodium azide
    Constituent: PBS
  • Concentration information loading...

  • 纯度

    Protein A purified

  • 纯化说明

    Purified from tissue culture supernatant.

  • 克隆

    单克隆

  • 克隆编号

    9H10

  • 骨髓瘤

    Sp2/0

  • 同种型

    IgG2b

  • 研究领域

应用

The Abpromise guarantee

Abpromise™承诺保证使用ab5832于以下的经测试应用

“应用说明”部分 下显示的仅为推荐的起始稀释度；实际最佳的稀释度/浓度应由使用者检定。

应用 Ab评论 说明
Flow Cyt
Use 1µg for 106 cells.

ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody.
IHC-P
Use a concentration of 1 µg/ml. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
ELISA
Use at an assay dependent concentration.
WB (3)
Use at an assay dependent concentration. Detects a band of approximately 34 kDa (predicted molecular weight: 38 kDa).
IP
Use at an assay dependent concentration. This antibody does not IP the hnRNP complex.
ICC/IF (2)
Use at an assay dependent concentration.

See Abreview (April 2, 2007).
说明
Flow Cyt
Use 1µg for 106 cells.

ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody.
IHC-P
Use a concentration of 1 µg/ml. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.
ELISA
Use at an assay dependent concentration.
WB
Use at an assay dependent concentration. Detects a band of approximately 34 kDa (predicted molecular weight: 38 kDa).
IP
Use at an assay dependent concentration. This antibody does not IP the hnRNP complex.
ICC/IF
Use at an assay dependent concentration.

See Abreview (April 2, 2007).

靶标

  • 功能

    Involved in the packaging of pre-mRNA into hnRNP particles, transport of poly(A) mRNA from the nucleus to the cytoplasm and may modulate splice site selection. May play a role in HCV RNA replication.

  • 序列相似性

    Contains 2 RRM (RNA recognition motif) domains.

  • 翻译后修饰

    Arg-194, Arg-206 and Arg-225 are dimethylated, probably to asymmetric dimethylarginine.
    Sumoylated.

  • 细胞定位

    Nucleus. Cytoplasm. Localized in cytoplasmic mRNP granules containing untranslated mRNAs. Shuttles continuously between the nucleus and the cytoplasm along with mRNA. Component of ribonucleosomes. In the course of viral infection, colocalizes with HCV NS5B at speckles in the cytoplasm in a HCV-replication dependent manner.
  • Information by UniProt

  • 数据库链接

    see all

  • 别名

    • HNRNPA 1 antibody
    • Helix destabilizing protein antibody
    • Helix-destabilizing protein antibody
    • Heterogeneous nuclear ribonucleoprotein A1 antibody
    • Heterogeneous nuclear ribonucleoprotein A1B protein antibody
    • Heterogeneous nuclear ribonucleoprotein B2 protein antibody
    • Heterogeneous nuclear ribonucleoprotein core protein A1 antibody
    • hnRNP A1 antibody
    • hnRNP core protein A1 antibody
    • HNRNPA1 antibody
    • HNRPA1 antibody
    • MGC102835 antibody
    • Nuclear ribonucleoprotein particle A1 protein antibody
    • ROA1_HUMAN antibody
    • Single strand DNA binding protein UP1 antibody
    • Single strand RNA binding protein antibody
    • Single-strand RNA-binding protein antibody
    see all

图片

  • Western blot - Anti-hnRNP A1 antibody [9H10] (ab5832)
    Western blot - Anti-hnRNP A1 antibody [9H10] (ab5832)
    All lanes : Anti-hnRNP A1 antibody [9H10] (ab5832) at 1 µg/ml

    Lane 1 : HeLa (Human epithelial carcinoma cell line) Whole Cell Lysate
    Lane 2 : Jurkat (Human T cell lymphoblast-like cell line) Whole Cell Lysate
    Lane 3 : HepG2 (Human hepatocellular liver carcinoma cell line) Whole Cell Lysate
    Lane 4 : HEK293 (Human embryonic kidney cell line) Whole Cell Lysate

    Lysates/proteins at 10 µg per lane.

    Secondary
    All lanes : Goat Anti-Mouse IgG H&L (HRP) preadsorbed (ab97040) at 1/5000 dilution

    Developed using the ECL technique.

    Performed under reducing conditions.

    Predicted band size: 38 kDa
    Observed band size: 37 kDa why is the actual band size different from the predicted?
    Additional bands at: 43 kDa. We are unsure as to the identity of these extra bands.


    Exposure time: 30 seconds
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP A1 antibody [9H10] (ab5832)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-hnRNP A1 antibody [9H10] (ab5832)
    Ab5832 staining human lung. Staining is localized to the nucleus.
    Left panel: with primary antibody at 1 ug/ml. Right panel: isotype control.
    Sections were stained using an automated system (Dako PT Link), at room temperature. Sections were rehydrated and antigen retrieved with the Dako 3-in-1 antigen retrieval buffer, citrate pH 6.0. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 minutes. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 minutes and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that for manual staining we recommend to optimize the primary antibody concentration and incubation time (overnight incubation), and amplification may be required.
  • Western blot - Anti-hnRNP A1 antibody [9H10] (ab5832)
    Western blot - Anti-hnRNP A1 antibody [9H10] (ab5832)This image is courtesy of an anonymous Abreview.
    All lanes : Anti-hnRNP A1 antibody [9H10] (ab5832) at 1/1000 dilution

    Lane 1 : Mouse NSC34 whole cell lysate with control siRNA
    Lane 2 : Mouse NSC34 whole cell lysate with hnRNP A1 siRNA

    Lysates/proteins at 10 µg per lane.

    Secondary
    All lanes : IRDye® 700DX-conjugated Donkey anti-Mouse IgG at 1/3000 dilution

    Performed under reducing conditions.

    Predicted band size: 38 kDa


    Exposure time: 1 minute


    Knockdown for 72 hours.

    See Abreview

  • Flow Cytometry - Anti-hnRNP A1 antibody [9H10] (ab5832)
    Flow Cytometry - Anti-hnRNP A1 antibody [9H10] (ab5832)
    Overlay histogram showing Jurkat cells stained with ab5832 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab5832, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in Jurkat cells fixed with 4% paraformaldehyde/permeabilized in 0.1% PBS-Tween used under the same conditions.

  • Immunoprecipitation - Anti-hnRNP A1 antibody [9H10] (ab5832)
    Immunoprecipitation - Anti-hnRNP A1 antibody [9H10] (ab5832)
    hnRNP A1 was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Mouse monoclonal to hnRNP A1 (ab5832) and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).
    The antibody was incubated under agitation with Protein G beads for 10min, Hela whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
    Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab5832.
    Secondary: Goat polyclonal to mouse IgG light chain specific (HRP) at 1/5000 dilution.
    Band: 37kDa: hnRNP A1; 42kDa:We are unsure as to the identity of this extra band.

文献 (52)

发表研究结果有使用 ab5832？请让我们知道，以便我们可以引用本数据表中的参考文章。

ab5832 被引用在 52 文献中.

  • Prophet SM  et al. p97/UBXD1 Generate Ubiquitylated Proteins That Are Sequestered into Nuclear Envelope Herniations in Torsin-Deficient Cells. Int J Mol Sci 23:N/A (2022). PubMed: 35563018
  • Luo Y  et al. KRAS mutant-driven SUMOylation controls extracellular vesicle transmission to trigger lymphangiogenesis in pancreatic cancer. J Clin Invest 132:N/A (2022). PubMed: 35579947
  • Zhang C  et al. Asiaticoside Suppresses Gastric Cancer Progression and Induces Endoplasmic Reticulum Stress through the miR-635/HMGA1 Axis. J Immunol Res 2022:1917585 (2022). PubMed: 35692504
  • Chen M  et al. PRMT5 regulates ovarian follicle development by facilitating Wt1 translation. Elife 10:N/A (2021). PubMed: 34448450
  • Chen C  et al. SUMOylation promotes extracellular vesicle-mediated transmission of lncRNA ELNAT1 and lymph node metastasis in bladder cancer. J Clin Invest 131:N/A (2021). PubMed: 33661764
View all Publications for this product

客户评价及客户问答

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1-7 of 7 Abreviews or Q&A

Western blot abreview for Anti-hnRNP A1 antibody [9H10]

 Excellent
Abreviews
Application
Western blot
Loading amount
15 µg
Gel Running Conditions
Non-reduced Non-Denaturing (Native) (4-12% Bis-Tris Gel, MES running buffer)
Sample
Human Cell lysate - whole cell (Human Embryonic Kidney)
Specification
Human Embryonic Kidney
Blocking step
BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Read More
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

Abcam user community

Verified customer

提交于 Mar 18 2014

Immunocytochemistry/ Immunofluorescence abreview for Anti-hnRNP A1 antibody [9H10]

 Inconclusive
Abreviews
abreview image
Application
Immunocytochemistry/ Immunofluorescence
Blocking step
Serum as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 10% · Temperature: 20°C
Sample
Rat Cell (oligodendrocytes)
Specification
oligodendrocytes
Permeabilization
Yes - 0,1%Triton X100
Fixative
Paraformaldehyde
Read More
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

Abcam user community

Verified customer

提交于 Jan 03 2014

Western blot abreview for Anti-hnRNP A1 antibody [9H10]

 Good
Abreviews
abreview image
Application
Western blot
Sample
Mouse Cell lysate - whole cell (NSC34)
Loading amount
10 µg
Specification
NSC34
Gel Running Conditions
Reduced Denaturing (4-12% nupage gel)
Blocking step
BSA as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 25°C
Read More
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

Abcam user community

Verified customer

提交于 Nov 13 2010

Immunocytochemistry/ Immunofluorescence abreview for Anti-hnRNP A1 antibody [9H10]

 Good
Abreviews
abreview image
Application
Immunocytochemistry/ Immunofluorescence
Sample
Human Cell (GM10725 Lymphoblastoid cell line)
Specification
GM10725 Lymphoblastoid cell line
Fixative
Paraformaldehyde
Blocking step
BSA as blocking agent for 30 minute(s) · Concentration: 5%
Read More
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

Abcam user community

Verified customer

提交于 Apr 02 2007

Western blot abreview for Anti-hnRNP A1 antibody [9H10]

 Excellent
Abreviews
Application
Western blot
Sample
Human Cell lysate - whole cell (cell type: IDH4)
Loading amount
5 µg
Specification
cell type: IDH4
Blocking step
Milk as blocking agent for 1 hour(s) and 0 minute(s) · Concentration: 10%
Read More
The reviewer received a reward from Abcam’s Loyalty Program in thanks for submitting this Abreview and for helping the scientific community make better-informed decisions.

Miss. Elizabeth Kovacs

Verified customer

提交于 Jun 06 2006

Question

Dear Tech Support Team, Our customer is willing to test ab5832 or ab10685 in IP with Drosophila samples. Are you interested in this type of the information for the Abreview promotion (The customer buys certain antibodies and upload Abreview on Abcam's website and then we give 100% credit note for this antibody to buy next antibody)? Do you have information about the homology of the immunogens of these 2 antibodies with Drosophila protein? Which of these two is preferable for the test withthe abreview promotion? Thanks in advance for your assistance and reply.

Read More
Answer

I have not been able to find the Drosophila sequence to check homology of the immunogen for either of these antibodies (full-length human hnRNP-A1) with the Drosophila sequence. This allows us to assess the likelihood of cross-reaction of the antibody with the untested species. I did find an apparent analog, the product of the Dm gene Hrb87F (Synonym: hrp36). Alignment of human hnRNP1 with this protein returns 57% identity. This suggests low potential for cross-reactivity (we look for 85% or better), but if your customer is still interested in trying one of these to IP Dm protein, I suggest ab5832, as there have been inconsistent results lately from ab10685. However, the antibody does not IP the hnRNP complex.

Read More

Question

BATCH NUMBER 132644 ORDER NUMBER -- NOT SPECIFIED -- DESCRIPTION OF THE PROBLEM no band detectable even after an exposure time of 20 min SAMPLE protein extract derived from peripheral blood mononuclear cells (PBMCs) PRIMARY ANTIBODY protein transfer to nitrocellulose membrane by wet blotting (over-night, 30V), standard transfer buffer based on methanol, after transfer: quality control by Ponceau-staining, blocking of membrane with 6% milk/TBS-Tween (based on non-fat dry milk) for 4 hours @ RT DETECTION METHOD SuperSignal West Pico Chemiluminescent Substrate (Pierce), detection with Hyperfilm ECL (Amersham) POSITIVE AND NEGATIVE CONTROLS USED the same membrane was stained with antibodies against beta-actin and SF2/ASF which worked great as usual; furthermore, the same protein extracts were used to stain SMN; hnRNP A1 is ubiquitously expressed and should therefore also be present in PBMCs; a positive control was not delivered with the antibody ANTIBODY STORAGE CONDITIONS as indicated SAMPLE PREPARATION isolation of PBMCs using BD Vacutainer? CPT Cell Preparation tubes, 2x washing of cells with 1xPBS, protein extraction with RIPA w/o protease inhibitors, sample storage @-80?C; volume corresponding to 7.5?g of protein/sample plus 2xLaemmli buffer, heating @95?C for 5 min, 12%SDS PAGE @50-100V for about 2.5h TRANSFER AND BLOCKING CONDITIONS protein transfer to nitrocellulose membrane by wet blotting (over-night, 30V), standard transfer buffer based on methanol, after transfer: quality control by Ponceau-staining, blocking of membrane with 6% milk/TBS-Tween (based on non-fat dry milk) for 4 hours @ RT SECONDARY ANTIBODY Peroxidase-conjugated Affiniti Pure Goat Anti-Mouse IgG (H+L)(competitor) 1:10.000 in 1.5% milk/TBS Tween (based on non-fat dry milk), @4?C, for 1h Washing: 5x5 min with TBS Tween HOW MANY TIMES HAVE YOU TRIED THE APPLICATION? 1 DO YOU OBTAIN THE SAME RESULTS EVERY TIME? No WHAT STEPS HAVE YOU ALTERED? An opportunity for alteration would be the use of higher amounts of the primary antibody, however, the total volume delivered is as low as 50 ?l. In our experimental set up, we used a 1:1000 dilution (10?l of antibody in 10ml total incubation volume). Switching to a 1:200 or 1:100 dilution is not possible with an antibody volume of 50?l delivered in total. Thus, alterations are only theoretically possible. ADDITIONAL NOTES the lab and me as investigator are experienced in the field of western blotting. no bands at all even after an exposure time of 20 min (besides of medium background which is present all over the blot) We would appreciate being reimbursed by another antibody aliquot of the same or another clone to hnRNP A1 which is working properly or by not paying for the aliquot we already got. A picture showing the result after 20 min exposure is available on request. Thank you very much for your efforts and your understanding!

Read More
Answer

Thank you for your enquiry. I am sorry to hear that your customer has been having problems with ab5832. Please thank them for taking the time to fill out our questionnaire. I have read their questionnaire and I have a few comments. Your protocol is not dissimilar to one that I would recommend for this antibody. I would also recommend a RIPA extraction given hnRNP A1 is a nuclear protein. We have had a favourable review posted recently for this antiserum by Naoko Tanese. His review did not appear to indicate anything that was performed differently from the standard conditions. However, given your protocol please may I suggest that you repeat this experiment, extracting your cells once again, just to rule out the fact that hnRNP A1 was not extracted by the RIPA buffer. It would also be of benefit to prolong the incubation time to overnight at 4oC and increasing the total mass of protein loaded onto the gel to 20ug. Also if possible change from Milk as a blocker to 5% BSA as this can give cleaner results. I think that keeping the dilution at 1:1000 is Ok as again Naoko Tanese, in his review obtained good results with this dilution. I think that combining these conditions would serve to give you the best chance of obtaining some favourable results. I look forward to hearing from you.

Read More

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