山羊抗兔IgG H&L (Alexa Fluor® 488)预吸附二抗(ab150081)

Abreviews (4) Submit a Question Specific References (11)

概述

  • 产品名称
    山羊抗兔IgG H&L (Alexa Fluor® 488)预吸附二抗
    参阅全部 IgG 二抗
  • 描述
    山羊多克隆抗体二抗to兔IgG - H&L (Alexa Fluor® 488),预吸附二抗
  • 宿主
    Goat
  • 靶标种属
    Rabbit
  • 特异性
    By immunoelectrophoresis and ELISA this antibody reacts specifically with rabbit IgG and with light chains common to other rabbit immunoglobulins. No antibody was detected against non-immunoglobulin serum proteins. Less than 0.1% cross reactivity to bovine, chicken, horse, human, mouse, pig, and rat IgG was detected. This antibody may cross react with IgG from other species.
  • 经测试应用
    适用于: IHC-Fr, ICC/IF, Flow Cyt, IHC-P, ELISAmore details
  • 最小交叉反应

    Human, Mouse, Rat more details
  • 免疫原

    The details of the immunogen for this antibody are not available.

  • 偶联物
    Alexa Fluor® 488. Ex: 495nm, Em: 519nm

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. Avoid freeze / thaw cycle.
  • 存储溶液
    Preservative: 0.02% Sodium azide
    Constituents: PBS, 30% Glycerol, 1% BSA
  • Concentration information loading...
  • 纯度
    Immunogen affinity purified
  • 纯化说明
    Antiserum was cross adsorbed using a human, mouse and rat immunosorbents to remove cross reactive antibodies. This antibody was isolated by affinity chromatography using antigen coupled to agarose beads.
  • 克隆
    多克隆
  • 同种型
    IgG
  • 常规说明

    Alexa Fluor® is a registered trademark of Molecular Probes, Inc, a Thermo Fisher Scientific Company. The Alexa Fluor® dye included in this product is provided under an intellectual property license from Life Technologies Corporation. As this product contains the Alexa Fluor® dye, the purchase of this product conveys to the buyer the non-transferable right to use the purchased product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). As this product contains the Alexa Fluor® dye the sale of this product is expressly conditioned on the buyer not using the product or its components, or any materials made using the product or its components, in any activity to generate revenue, which may include, but is not limited to use of the product or its components: in manufacturing; (ii) to provide a service, information, or data in return for payment (iii) for therapeutic, diagnostic or prophylactic purposes; or (iv) for resale, regardless of whether they are sold for use in research. For information on purchasing a license to use products containing Alexa Fluor® dyes for purposes other than research, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad, CA 92008 USA or outlicensing@lifetech.com.

  • 研究领域

应用

Our Abpromise guarantee covers the use of ab150081 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

应用 Ab评论 说明
IHC-Fr Use at an assay dependent concentration.
ICC/IF 1/200 - 1/1000.
Flow Cyt 1/2000 - 1/4000.
IHC-P Use at an assay dependent concentration.
ELISA Use at an assay dependent concentration.

图片

  • Immunocytochemistry/ Immunofluorescence - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)
    Immunocytochemistry/ Immunofluorescence - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)

    ICC/IF image of ab8227 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab8227, 5µg/ml) overnight at +4°C. The secondary antibody (green) was ab150081 Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at 2µg/ml for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.

    The negative control (inset) is a secondary-only assay to demonstrate low non-specific binding of the secondary antibody.

  • Immunohistochemistry (Frozen sections) - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)
    Immunohistochemistry (Frozen sections) - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)This image is courtesy of an abreview submitted by Bryan Niedenberger

    Postnatal day 6 mouse testes were fixed with 4% paraformaldehyde. Tissue was embedded in O.C.T. and frozen. 5 micron sections were cut and transferred to slides. Sections were permeabilized with 0.1% Triton X-100 in PBS, and blocked with 3% BSA in 0.1% Triton X-100 + PBS. Sections were incubated with either (A) no primary antibody or (B ) anti-DDX4 (ab13840) for 1 h at RT. Sections were then washed 3X with 0.1% Triton X-100 in PBS and Goat-Anti Rabbit 488 (ab150081) applied at a 1/500 dilution. Sections were then mounted after washing 3X with 0.1% Triton X-100 in PBS.

  • Immunohistochemistry (Frozen sections) - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)
    Immunohistochemistry (Frozen sections) - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)This image is courtesy of Dr. Shaohua Li

    Image: Courtesy of Dr. Shaohua Li, UMDNJ-Robert Wood Johnson Medical School

    Sample: mouse embryonic stem cell-differentiated embryoid bodies (EBs)

    Preparation:

    Fix in 3%PFA in PBS for 30 min at RTIncubate in 7.5% sucrose-PBS for 3h at RTIncubate in 15% sucrose-PBS at 4 degree Celsius overnightEmbed the EBs in tissue-Tek OCT compoundCut frozen sections to 4-20 µm thickness

    Primary antibody 1: Rabbit anti cytokeratin 8 (ab53280), 1:100

    Primary antibody 2: Rat anti-perlecan, 1:100 
    Secondary antibody 1: Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) pre-adsorbed (ab150081), 1:200

    Secondary antibody 2: Goat polyclonal Secondary Antibody to Rat IgG - H&L (Cy5®) pre-adsorbed, 1:200
    Nuclei were counterstained with DAPI 

  • Flow Cytometry - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)
    Flow Cytometry - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)
    Overlay histogram showing Jurkat cells stained with ab16669 (red line). The cells were fixed with 4% paraformaldehyde (10 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 (ab16669, 1/1000 dilution) for 30 min at 22°C. The secondary antibody Goat anti-rabbit IgG H&L (Alexa Fluor® 488, pre-adsorbed) (ab150081) was used at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monclonal) (0.1μg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter.
  • Alexa Fluor® - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)
    Alexa Fluor® - Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed (ab150081)

文献

This product has been referenced in:
  • Guo L  et al. An adaptable chromosome preparation methodology for use in invertebrate research organisms. BMC Biol 16:25 (2018). Read more (PubMed: 29482548) »
  • Divan A  et al. Borrelia burgdorferi adhere to blood vessels in the dura mater and are associated with increased meningeal T cells during murine disseminated borreliosis. PLoS One 13:e0196893 (2018). Read more (PubMed: 29723263) »

See all 11 Publications for this product

发表研究结果有使用 ab150081？请让我们知道，以便我们可以引用本数据表中的参考文章。

客户评价及客户问答

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4 reviews or Q&A

10
Votes: Highest First

good working antibody

 Good
Abreviews
Application
Immunocytochemistry/ Immunofluorescence
We used the antibody together with the ab38578 antibody (Siglec8) on cytospins with eosinophilic granulocytes.
The working concentration was 1/100 for 30 minutes at room temperature.
abreview image
Username

Abcam user community

Verified customer

提交于 Feb 14 2018

Excellent results

 Excellent
Abreviews
Application
Immunohistochemistry (Frozen sections)
I have used this antibody at a 1:500 dilution with many different primary antibodies. It works well and and gives a bright signal with no discernible nonspecific staining.
Postnatal day 6 mouse testes were fixed with 4% paraformaldehyde. Tissue was embedded in O.C.T. and frozen. 5 micron sections were cut and transferred to slides. Sections were permeabilized with 0.1% Triton X-100 in PBS, and blocked with 3% BSA in 0.1% Triton X-100 + PBS. Sections were incubated with either (A) no primary antibody or (B ) anti-DDX4 (Abcam ab13840) for 1 h at RT. Sections were then washed 3X with 0.1% Triton X-100 in PBS and Goat-Anti Rabbit 488 (Abcam ab150081) applied at a 1:500 dilution. Sections were then mounted after washing 3X with 0.1% Triton X-100 in PBS.
abreview image
Username

Mr. Bryan Niedenberger

Verified customer

提交于 Mar 09 2016

Indirect Immunofluorescent labeling of a nuclear lamin protein

 Excellent
Abreviews
Application
Immunocytochemistry/ Immunofluorescence
This antibody has been used extensively with a number of different primary antibodies generated in rabbits. It performs extremely well at a 1:200 dilution.
Attached is an immunofluorescent image of MeOH-fixed HeLa cells that were immunofluorescently labeled with a Lamin A/C (nuclear membrane) antibody (ab133256). The secondary antibody has been pseudo-colored green in the merged image. DNA was counterstained with DAPI.
abreview image
Username

Dr. Kirk Mcmanus

Verified customer

提交于 Mar 28 2014

Good secondary a.b. for IHC (PFA-Fixed Flash-Frozen sections)

 Good
Abreviews
Application
Immunohistochemistry
Application: Immunohistochemistry (PFA perfusion fixed frozen sections) or IHC(FoFr)

I used this antibody on PFA fixed, sucrose cryoprotected frozen sections from the mouse brain (below is a brief description). The primary a.b. I used was anti-mGluR5 (ab53090), which was somewhat difficult to get working.

Full Description:
Transcardially perfused the mouse with 4% PFA. Dissected the brain and placed in PFA for a few hours later, placed in 30% sucrose overnight for cryoprotection. Then, snap/flash froze the brain and used a cryostat for sectioning into 20 micron coronal slices. Applied primary anti-mGluR5 (ab53090) antibody, followed by the secondary antibody (dilution: 1/200), according to standard protocols. No blocking, no antigen-retrieval, and no permeabilization was done.
abreview image
Username

Abcam user community

Verified customer

提交于 Jan 29 2014

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