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Anti-Caveolin-1 antibody - Caveolae Marker

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100ug
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产品详情
  • 产品名称

    Anti-Caveolin-1抗体- Caveolae Marker
    参阅全部 Caveolin-1 一抗

  • 描述

    兔多克隆抗体to Caveolin-1 - Caveolae Marker

  • 宿主

    Rabbit

  • 经测试应用

    适用于: WBICC/IFIPmore details

  • 种属反应性

    与反应: Mouse, Rat, Human
    预测可用于: Sheep, Rabbit, Horse, Cow, Cat, Pig, Chimpanzee, Gorilla, African green monkey, African bush elephant

  • 免疫原

    Synthetic peptide corresponding to Human Caveolin-1 aa 1-100.
    Database link: 
    Q03135

    Run BLAST with BLAST the sequence with ExPASyRun BLAST with BLAST the sequence with NCBI

  • 阳性对照

    • WB: Human lung, heart and spleen tissue lysates; Mouse heart and lung tissue lysates; Rat heart protein extract; PANC-1, U-87 MG, A549, HeLa, PC-3, U-2 OS, C2C12 and A431 cell lysates. ICC/IF: A-375, HeLa and NIH/3T3 cells; Rat astrocytes.

  • 常规说明

    This antibody can be used as a marker for lipid raft fractions.


    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

The Abpromise guarantee

Abpromise™承诺保证使用ab2910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
WB(21)

Use a concentration of 1 - 2 µg/ml. Detects a band of approximately 22 kDa (predicted molecular weight: 20 kDa).

ICC/IF(15)

Use at an assay dependent concentration.

IP(9)

Use at an assay dependent concentration. 

Recommended dilution: 5 µg

数据库链接

别名

  • BSCL3 antibody

  • CAV antibody

  • CAV1 antibody

  • CAV1_HUMAN antibody

  • caveolae protein, 22 kD antibody

  • caveolin 1 alpha isoform antibody

  • caveolin 1 beta isoform antibody

  • Caveolin 1 caveolae protein 22kDa antibody

  • Caveolin-1 antibody

  • Caveolin1 antibody

  • cell growth-inhibiting protein 32 antibody

  • CGL3 antibody

  • LCCNS antibody

  • MSTP085 antibody

  • OTTHUMP00000025031 antibody

  • PPH3 antibody

  • VIP 21 antibody

  • VIP21 antibody

  • Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    All lanes : Anti-Caveolin-1 antibody - Caveolae Marker (ab2910) at 1.5 µg/ml

    Lane 1 : Human lung
    Lane 2 : Human heart
    Lane 3 : Human spleen

    Lysates/proteins at 20 µg per lane.

    Secondary
    All lanes : Alexa Fluor anti-rabbit at 1/5000 dilution

    Predicted band size: 20 kDa
    Observed band size: 20 kDa

  • Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    ab2910 staining Caveolin-1 in wild-type HeLa cells (top panel) and CAV1 knockout HeLa cells (ab255371) (bottom panel). The cells were fixed with 100% methanol (5 min) then permeabilized with 0.1% Triton X-100 for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1% PBS-Tween for 1h. The cells were then incubated with ab2910 at 1/500 dilution and ab7291 (Mouse monoclonal to alpha Tubulin) at 1/1000 dilution overnight at 4°C followed by a further incubation at room temperature for 1h with a goat secondary antibody to rabbit IgG (Alexa Fluor® 488) (ab150081) at 2 μg/ml (shown in green) and a goat secondary antibody to mouse IgG (Alexa Fluor® 594) (ab150120) at 2 μg/ml (shown in red). Nuclear DNA was labelled in blue with DAPI.
    Image was taken with a confocal microscope (Leica-Microsystems TCS SP8).

  • Immunoprecipitation - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Immunoprecipitation - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Caveolin 1 was immunoprecipitated using 5 µg of ab2910 from lysate of Mouse Heart (Lane 3) using the Dynabeads® Protein A Immunoprecipitation Kit. Normal Rabbit IgG was used as a Isotype control (Lane 2). 10 % input represents the cell extract used for immunoprecipitation (Lane 1). Western blot analysis was performed using Caveolin 1 Rabbit Polyclonal Antibody and Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate. Chemiluminescent detection was performed using Pierce™ ECL Western Blotting Substrate.



    All lanes :

    Lane 1 : Input control
    Lane 2 : Isotype control
    Lane 3 : IP elute

  • Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    All lanes : Anti-Caveolin-1 antibody - Caveolae Marker (ab2910) at 1 µg/ml

    Lane 1 : CAV1 knockout HeLa cell lysate
    Lane 2 : Wild-type HeLa cell lysate

    Predicted band size: 20 kDa



    The specificity of ab2910 was demonstrated by CRISPR targeted CAV1 knockout in HeLa cells. Western blot analysis of whole cell lysates using this antibody showed no detection of caveolin 1 protein expression in knockout cells compared to the protein detected at ~22kDa in wild-type HeLa cells. 

    Knockout validation info.

  • Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    All lanes : Anti-Caveolin-1 antibody - Caveolae Marker (ab2910) at 1 µg/ml

    Lane 1 : PANC-1 (Human pancreatic epithelial cancinoma cell line) whole cell lysate
    Lane 2 : U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) whole cell lysate
    Lane 3 : A549 (Human lung carcinoma cell line) whole cell lysate
    Lane 4 : HeLa (Human cervix adenocarcinoma epithelial cell) whole cell lysate
    Lane 5 : PC-3 (Human prostate adenocarcinoma cell line) whole cell lysate
    Lane 6 : U-2 OS (Human bone osteosarcoma epithelial cell line) whole cell lysate
    Lane 7 : Mouse heart tissue lysate
    Lane 8 : Rat heart tissue lysate
    Lane 9 : C2C12 (Mouse myoblast cell line) whole cell lysate
    Lane 10 : Mouse lung tissue lysate
    Lane 11 : A-431 (Human epidermoid carcinoma cell line) whole cell lysate

    Lysates/proteins at 20 µg per lane.

    Predicted band size: 20 kDa



    Western blot analysis was performed on whole cell extracts (20 µg lysate). The blots were probed with Anti-ab2910 (1-2 µg/mL) and detected by chemiluminescence using Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate. A 17 kDa band corresponding to Caveolin-1 was observed across cell lines and tissues tested. Known quantity of protein samples were electrophoresed using Novex® NuPAGE® 12 % Bis-Tris gel, XCell SureLock™ Electrophoresis System and Novex® Sharp Pre-Stained Protein Standard. Resolved proteins were then transferred onto a nitrocellulose membrane with iBlot® 2 Dry Blotting System. The membrane was probed with the relevant primary and secondary Antibody following blocking with 5 % skimmed milk. Chemiluminescent detection was performed using Pierce™ ECL Western Blotting Substrate.

  • Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Western blot - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Anti-Caveolin-1 antibody - Caveolae Marker (ab2910) at 2 µg/ml + Rat heart protein extract

    Predicted band size: 20 kDa

  • Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Immunofluorescence analysis of Caveolin 1 was done on 70% confluent log phase A-375 cells. The cells were fixed with 4% paraformaldehyde for 15 minutes, permeabilized with 0.25% Triton™ X-100 for 10 minutes, and blocked with 5% BSA for 1 hour at room temperature. The cells were labeled with ab2910 at 1 µg/mL in 1% BSA and incubated for 3 hours at room temperature and then labeled with Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate at a dilution of 1:2000 for 45 minutes at room temperature (Panel a: green). Nuclei (Panel b: blue) were stained with SlowFade® Gold Antifade Mountant with DAPI. F-actin (Panel c: red) was stained with Alexa Fluor® 555 Rhodamine Phalloidin. Panel d is a merged image showing cytoplasmic localization. Panel e is a no primary antibody control. The images were captured at 60X magnification.

  • Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Rat astrocytes stained with fluorescently labeled Caveolin-1 antibody.

    Primary antibody is ab2910 at a dilution of 1/500 and the secondary antibody is Texas red labeled anti-rabbit IgG at a dilution of 1/1000.

    This image was kindly supplied as part of the review submitted by Donghui Zhu.

  • Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)

    Immunocytochemistry/ Immunofluorescence - Anti-Caveolin-1 antibody - Caveolae Marker (ab2910)This image is courtesy of an anonymous Abreview

    ab2910 staining Caveolin-1 - Caveolae Marker in HeLa (Human epithelial cell line from cervix adenocarcinoma) cells by ICC/IF (Immunocytochemistry/immunofluorescence).

    Cells were fixed with paraformaldehyde. Samples were incubated with primary antibody (1/200 in PBS + 0.05% Saponin) for 1 hour at 37°C. A Cy3®-conjugated Donkey anti-rabbit polyclonal (1/500) was used as the secondary antibody.

    See Abreview