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山羊抗小鼠IgG H&L (FITC)预吸附二抗(ab7064)

Reviews (3)Q&A (2)References (36)
Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
  • Flow Cytometry - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
  • Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)

Key features and details

  • Goat Anti-Mouse IgG H&L (FITC) preadsorbed
  • Conjugation: FITC. Ex: 493nm, Em: 528nm
  • Host species: Goat
  • Isotype: IgG
  • Suitable for: WB, Dot blot, ICC/IF, Immunomicroscopy, Flow Cyt, IHC-P, IHC-Fr, ELISA

概述

  • 产品名称

    山羊抗小鼠IgG H&L (FITC)预吸附二抗
    参阅全部 IgG 二抗

  • 宿主

    Goat

  • 靶标种属

    Mouse

  • 特异性

    No reaction was observed against Bovine, Chicken, Goat, Guinea Pig, Hamster, Horse, Human, Rabbit, Rat and Sheep Serum Proteins.

  • 经测试应用

    适用于: WB, Dot blot, ICC/IF, Immunomicroscopy, Flow Cyt, IHC-P, IHC-Fr, ELISAmore details

  • 最小交叉反应


    Chicken, Cow, Goat, Guinea pig, Hamster, Horse, Human, Rabbit, Rat, Sheep more details

  • 免疫原

    Full length native Mouse IgG (purified).

  • 偶联物

    FITC. Ex: 493nm, Em: 528nm

性能

  • 形式

    Liquid

  • 存放说明

    Shipped at 4°C. Store at +4°C.

  • 存储溶液

    pH: 6.50
    Preservative: 0.01% Sodium azide
    Constituents: 0.42% Tripotassium orthophosphate, 0.87% Sodium chloride, 1% BSA
  • Concentration information loading...

  • 纯度

    Affinity purified

  • 纯化说明

    Goat Anti-Mouse IgG was prepared from monospecific antiserum by immunoaffinity chromatography using Mouse IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities.

  • 克隆

    多克隆

  • 同种型

    IgG

  • 研究领域

相关产品

应用

The Abpromise guarantee

Abpromise™承诺保证使用ab7064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
Use at an assay dependent concentration. Predicted molecular weight: 36 kDa.
Dot blot
Use at an assay dependent concentration.
ICC/IF (1)
Use at an assay dependent concentration. PubMed: 15767251
Immunomicroscopy
Use at an assay dependent concentration.
Flow Cyt (1)
1/1000 - 1/2000.
IHC-P
Use at an assay dependent concentration.
IHC-Fr (1)
Use at an assay dependent concentration.
ELISA
1/10000 - 1/50000.
说明
WB
Use at an assay dependent concentration. Predicted molecular weight: 36 kDa.
Dot blot
Use at an assay dependent concentration.
ICC/IF
Use at an assay dependent concentration. PubMed: 15767251
Immunomicroscopy
Use at an assay dependent concentration.
Flow Cyt
1/1000 - 1/2000.
IHC-P
Use at an assay dependent concentration.
IHC-Fr
Use at an assay dependent concentration.
ELISA
1/10000 - 1/50000.

图片

  • Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
    Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)Humphries, W.H. 4th et al PLoS One. 2011;6(10):e26626. doi: 10.1371/journal.pone.0026626. Epub 2011 Oct 24 Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

    Rab7 and LAMP1 are highly colocalized in BS-C-1 cells and in HeLa cells

    LAMP1  was detected with a mouse antiLAMP1 antibody in ICC/IF analysis of BS-C-1 cells.

    Anti-LAMP1 was visualized using ab7064 at 1/500 diulution.

  • Flow Cytometry - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
    Flow Cytometry - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
    Overlay histogram showing Jurkat cells stained with ab8090 (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 (ab8090, 0.01μg/1x106 cells) for 30 min at 22°C. The secondary antibody Goat anti-mouse IgG H&L (FITC, pre-adsorbed) (ab7064) was used at 1/1000 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 0.01μg/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.
  • Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
    Immunocytochemistry/ Immunofluorescence - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)

    ab7064 was used at dilution 1/20 with the primary antibody ab7852 in ICC. See the review on ab7852.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Goat Anti-Mouse IgG H&L (FITC) preadsorbed (ab7064)

    ab7064 was used at dilution 1/2000 with the primary antibody ab2378 in IHC-P. See the review on ab2378.

实验方案

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.

Click here to view the general protocols

文献 (36)

发表研究结果有使用 ab7064？请让我们知道，以便我们可以引用本数据表中的参考文章。

ab7064 被引用在 36 文献中.

  • Smith EJ  et al. Tumour necrosis factor alpha, interleukin 1 beta and interferon gamma have detrimental effects on equine tenocytes that cannot be rescued by IL-1RA or mesenchymal stromal cell-derived factors. Cell Tissue Res 391:523-544 (2023). PubMed: 36543895
  • Mondello C  et al. Postmortem Biochemistry and Immunohistochemistry in Anaphylactic Death Due to Hymenoptera Sting: A Forensic Case Report. Int J Environ Res Public Health 20:N/A (2023). PubMed: 37174160
  • Takakura D  et al. Comprehensive Membrane N-Glycoproteomics Using Human Breast Cancer Cell Line Pairs. Mass Spectrom (Tokyo) 12:A0117 (2023). PubMed: 37250596
  • Ieni A  et al. Immunoexpression of p62/SQSTM1/Sequestosome-1 in human primary and recurrent IDH1/2 wild-type glioblastoma: A pilot study. Oncol Lett 24:336 (2022). PubMed: 36039055
  • Coppola L  et al. KCTD15 Is Overexpressed in her2+ Positive Breast Cancer Patients and Its Silencing Attenuates Proliferation in SKBR3 CELL LINE. Diagnostics (Basel) 12:N/A (2022). PubMed: 35328144
View all Publications for this product

客户评价及客户问答

Show All 评价 Q&A
提交评价 提交问题

1-5 of 5 Abreviews or Q&A

nice working antibody

 Good
Abreviews
Application
Immunohistochemistry (Frozen sections)
This is a good antibody and a stable conjugate.
The binding is specific.
The luminous intensity of the conjugate is good and is stable (can still be evaluated after a long time).
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 Oct 07 2015

good secendary antibody

 Good
Abreviews
Application
Flow Cytometry
This is a good functioning antibody with a stable conjugate.
The binding is very specific and the luminous intensity of the conjugate is good.
We have used it in the flow cytometry with a 1/1000 dilution
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 Oct 06 2015

Talin Staining

 Good
Abreviews
abreview image
Application
Immunocytochemistry/ Immunofluorescence
Mouse Osteoblast cells were grown on cover slips for 48 hrs. Then Cells were fixed with formaldehyde vapor for 10 mins. Cells were permeabilized with Triton-X 100 for 5-7mins. 3% BSA was used for blocking (1hr). 1:100 dilution of mouse anti-talin antibody to mouse was added onto the cells and incubated for 1hr. Then 1:500 dilution of anti-mouse FITC conjugated secondary antibody was added on to the cells and incubated for 1hr. Before proceeding to each step cells were washed with PBS.
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 Jul 05 2013

Question

Thanks for your kindly reply, this customer already tried to used the other secondary antibody ab6785 (Goat polyclonal Secondary Antibody to Mouse IgG - H&L (FITC)) to conducted the same experiment, but the result still shows weak signal, therefore, she think these antibodies was lost its function already, I also attached the results in this letter, please check it and could you please help this customer to create two credit notes? I am really appreciate for your kindly help : )

Best regards

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Answer

Thank you for confirming this details.

In my understanding this results show that the ab24590 isfaulty as it has been used with two different secondary antibodies without success. I provide you here therefore with the credit note for this antibody. The credit note ID is xxfor the ab24590.

In regards to the ab7064, I expect this antibody to work with another primary mouse antibody.I do not think that this antibody also should be faulty. Pleasedo let me knowhowever if you have anyconcerns in this regards.

Thank you for your help and cooperation also in this case.Please let me know if you have any questions.

Read More

Question

xx product code: ab24590, ab7064 ˙Antibody storage conditions (temperature/reconstitution etc) : -20℃ 2) Please describe the problem (high background, non-specific signal…etc). No staining 3) On what material are you testing the antibody in IHC/ICC? ˙Species: Human ˙What’s cell line or tissue: HUVEC (cell line, P4) 4) Sample preparation: ˙Type of sample (Fresh frozen sections, perfusion fixed frozen sections, PFA/formalin fixed ˙paraffin embedded sections, cells in culture, other:____) : cells in culture with 2% gelatin coating ˙Sample preparation: ˙Positive control : ˙Negative control : 5) Fixation step ˙Yes or No : Yes and no, both way are tried ˙If yes, Fixative agent and concentration: 4% PFA ˙Fixation time: 10min ˙Fixation temperature : room temperature 6) Antigen retrieval method(including time, temperature etc.): no ˙Did you do a permeabilization step (details please) or add permeabilizing agent in any dilution buffers? Yes if fixation is done and no if not fixed ˙Permeabilizing agent and concentration: 0.2% Tween20 after fixation 8) Blocking agent (eg BSA, serum…): ˙Concentration:1%BSA/PBS ˙Blocking time : 30min ˙Blocking temperature: room temperature 9) ˙Endogenous peroxidases blocked? no ˙Endogenous biotins blocked? no 10) Primary antibody (If more than one was used, describe in “additional notes”) : ˙Species: mouse ˙Reacts against: human ˙At what dilution(s) have you tested this antibody: 1:50 and 1:100 ˙Diluent buffer: 1%BSA/PBS ˙Incubation time: 1 hr and 2hr at room temperature or 4°C overnight ˙What washing steps were done (which buffer, number of washes): PBS X3 5min 11) Secondary antibody: gout anti mouse IgG(H+L) (ab7064) ˙Species: goat ˙Reacts against which species: mouse ˙At what dilution(s) have you tested this antibody: 1:20 1:50 and 1:100 ˙Diluent buffer: 1%BSA/PBS ˙Incubation time: 1hr at room temperature ˙What washing steps were done (which buffer, number of washes): PBS X3 5min ˙Fluorochrome or enzyme conjugate (eg: FITC, HRP, AP, biotin…etc): FITC ˙Do you know whether the problems you are experiencing come from the secondary? 12) Signal amplification method (eg: ABC, LSAB, HRP polymer, TSE): 13) Detection method (eg: DAB, BCIP/NBT …etc): Slides were observed under a fluorescence microscope and confocal microscope 14) ˙ How many times have you run this staining? 5 times ˙Do you obtain the same results every time? yes ˙What steps have you altered to try and optimize the use of this antibody? Dilutions of the primary antibody and secondary antibody Incubation time of primary antibody Fixation or no fixation

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Answer

Thank you for taking time to complete our questionnaire and for contacting us. I am sorry to hearthat the customer is notobtaining a staining with this two antibodies.

The details provided will enable us to investigate this case and will provide us with vital information for monitoring product quality. I appreciate the time the customer has spent in the laboratory. It is regrettable the results have not been successful.

Having reviewed the protocol details, I believe these two products should have given satisfactory results. It appears that you may have received a faulty vial. I apologize for the inconvenience and am pleased to offer you a free of charge replacement, credit note, or refund in compensation.In order however to replace the right antibody, we need toknow whether the primary or the secondary antibody is faulty. Can the customer therefore either test the secondary antibody with another mouse primary antibody which is known to work, or alternatively use another secondary antibody witht hte ab24590 to see whether the problem is due to the secondary antibody?

Thank you for your cooperation. I look forward to hearing from you.

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