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Rabbit Anti-Goat IgG H&L (Biotin) (ab6740)

Submit a review Q&A (2)References (17)

Key features and details

  • Rabbit Anti-Goat IgG H&L (Biotin)
  • Conjugation: Biotin
  • Host species: Rabbit
  • Suitable for: Dot blot, ELISA, IHC-P, IHC-Fr, Immunomicroscopy, ICC/IF, WB

Conjugates logo Related conjugates and formulations

Alexa Fluor® 405 Alexa Fluor® 488 Alexa Fluor® 555 Alexa Fluor® 568 Alexa Fluor® 594 Alexa Fluor® 647 Alkaline Phosphatase beta-galactosidase DyLight® 488 FITC Glucose Oxidase HRP TRITC Unconjugated Unconjugated

製品の概要

  • 製品名

    Rabbit Anti-Goat IgG H&L (Biotin)
    IgG 二次抗体 製品一覧

  • 由来種

    Rabbit

  • ターゲット生物種

    Goat

  • アプリケーション

    適用あり: Dot blot, ELISA, IHC-P, IHC-Fr, Immunomicroscopy, ICC/IF, WBmore details

  • 免疫原

    Goat IgG whole molecule

  • 標識

    Biotin

製品の特性

  • 製品の状態

    Liquid

  • 保存方法

    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.

  • バッファー

    pH: 6.50
    Preservative: 0.01% Sodium azide
    Constituents: 0.42% Tripotassium orthophosphate, 0.88% Sodium chloride, 1% BSA
  • Concentration information loading...

  • 精製度

    Affinity purified

  • 特記事項（精製）

    Goat Secondary Antibodies are prepared from monospecific antiserum by immunoaffinity chromatography using Goat IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities.

  • 特記事項（標識）

    Biotinamidocaproate N-Hydroxysuccinimide Ester (BAC) Biotin/Protein Ratio: 10-20 BAC molecules per Rabbit IgG molecule

  • ポリ/モノ

    ポリクローナル

  • 研究分野

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ab6740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
Dot blot
ELISA
IHC-P
IHC-Fr
Immunomicroscopy
ICC/IF
WB
特記事項
追加情報
Dot: Use at an assay dependent dilution.
ELISA: Use at an assay dependent dilution.
IHC-P: 1/100 (PMID 18930986).
IHC-Fr: Use at an assay dependent dilution.
IM: Use at an assay dependent dilution.
WB: Use at an assay dependent dilution.


Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.

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.

Click here to view the general protocols

参考文献 (17)

ab6740 を使用した論文を発表された方は、こちらまでお知らせください。データシートに掲載させていただきます。

ab6740 は 17 報の論文で使用されています。

  • Costa GMJ  et al. High SARS-CoV-2 tropism and activation of immune cells in the testes of non-vaccinated deceased COVID-19 patients. BMC Biol 21:36 (2023). PubMed: 36797789
  • Farias TO  et al. Testis and brown adipose tissue xenografts from yellowish myotis (Myotis levis). Reprod Fertil 3:287-300 (2022). PubMed: 36331914
  • Scheld M  et al. Modulatory effect of 17ß-estradiol on myeloid cell infiltration into the male rat brain after ischemic stroke. J Steroid Biochem Mol Biol 202:105667 (2020). PubMed: 32407868
  • de Oliveira CFA  et al. Comparative testis structure and function in three representative mice strains. Cell Tissue Res 382:391-404 (2020). PubMed: 32666138
  • Wang Z  et al. TRPV4-induced inflammatory response is involved in neuronal death in pilocarpine model of temporal lobe epilepsy in mice. Cell Death Dis 10:386 (2019). PubMed: 31097691
View all Publications for this product

レビューと Q&A

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レビューを送る 質問を送る

1-2 of 2 Abreviews or Q&A

Question

I wish to use this secondary reagent as part of an IHC experiment on frozen and PPFE rat muscle. I tried a rabbit anti-goat:biotin from Dako but this gave an unacceptable level of backgound. You state in the purification notes that the antibody is adsorbed against other impurities, does this include rat tissue?

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Answer

Thank you for your enquiry. This antibody has not been preadsorbed against rat tissue. In your case I would recommend ab7124 as this is a donkey polyclonal to goat IgG H&L (biotin-conjugated) pre-adsorbed antibody that has minimum cross reactivity to Chicken, Guinea Pig, Hamster, Horse, Mouse, Rabbit and Rat Serum Proteins. Using the rabbit antibody on rat tissue is very difficult because these species are very close and there is often high background. ab7124 should be better for your purposes. I hope this information helps, please do not hesitate to contact us if you need any more advice or information,

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Question

Thanks for your reply. Please see responses below. Apologies, but I don't have the PO number immediately available. The lot number is 48073. 1. Please describe the problem (high background, low signal, no signal etc). There does appear to be high background with the combination of ab1664, the ab6740 secondary, and a strepavidin-fluorophore from Pharmingen. I've tried strepavidin-PE, APC, TexasRed, etc. 2. On what material are you testing the antibody in FACS? •Species? •Cell type? •Cell line? I've been looking at epidermal cells from B6 mouse ear, gating on scatter characteristics, then CD45+ CD3+ (T-cells), and looking for CCR4 positive cells. 3. Which buffer did you use for cell suspension? We stain in FACS buffer, which is normal PBS + 2% FCS + 0.05% sodium azide. 4. How many cells did you use? ~1 million epidermal cells per sample. 5. Did you permeabilize the cells? How? No. 6. Primary antibody •Specification (in which species was it raised against)? •At what dilution(s) have you tested this antibody? •Incubation time, wash steps (multiple short washes are more effective than fewer longer wash steps)? Dilution is 1 microliter of ab1664 per 50 microliters (the volume we stain in). We incubate for ~15 to 30 minutes. We then wash with FACS buffer (PBS + sodium azide + FCS), and then repeat the staining procedure with the secondary rabbit antibody and strepavidin+fluorophore tertiary. 7. Secondary antibody •What secondary antibody are you using? •Specification (in which species was it raised against)? •At what dilution(s) have you tested this antibody? •Incubation, wash steps? •Do you know whether the problems you are experiencing come from the secondary? •What detection method are you using? ab6740, also dilution of 1 microliter of ab6740 per 50 microliters for a stain of one million cells, as above. Washing is as above. I then apply the strepavidin-fluorophore at the same dilution and incubate (again usually about 15 minutes). This is followed by a final wash. We usually FACS 1 million cells in a final volume of 200 microliters. 8. Which detection system did you use? •Detection wavelength The machine is a BD biosciences LSR 1. I've used a variety of fluorophores, corresponding to multiple wavelengths for FITC, PE, TexasRed, APC, and APC/Cy7. 9. Did you apply positive and negative controls along with the samples? Please specify. Negative controls has been splenocytes from normal B6 mice, which are expected to have cells that largely lack mCCR4. No positive controls have been really available. The strepavidin-fluorophores are known to work as they're widely used with a number of other biotinylated antibodies (admittedly many from Pharmingen). The rabbit anti goat secondary hssn't been tested because the only other goat antibody we have is ab1661 (anti-CCR10 and not advertised by Abcam as suitable for FACS. Been having the same issues with that one as well, but that's a different story). 10. Optimization attempts •How many times have you tried the FACS? •Do you obtain the same results every time? •What steps have you altered? Have tried the FACS 3 or 4 times. I've maintainly altered procedures for the collection of epidermal cells, but haven't really tried changing the FACS staining or acquisition steps.

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Answer

Thank you very much for your patience and for the details in which you have provided. I contacted the originator of ab1664 and below is the FACS protocl that they used. I hope this will be of use to you and if you continue to experience difficulty with this antibody please let me know and I will send you a replacement or a refund. FACS Protocol: 1. Pellet approx. 200,000 cells by centrifugation. 2. Resuspend the cell pellet in 50-75ul of medium with 5% FBS. 3. Add 1-5 ul of the anti-CCR antibody. 4. Incubate at 4 degree C for 45 minutes. 5. Wash the cells two or more times before adding secondary antibody. 6. Try using FITC conjugated F(ab’)2 anti goat antibody at appropriate dilution. If using anti-goat IgG then a blocking step indicated below is strongly recommended to reduce non-specific background. 7. Wash the cells and analyze. Controls and Blocking Steps: 1. Blocking of Fc-receptors: If one intends to use secondary IgG antibody raised in rabbits then the investigator initially should pre-incubate mouse cells with normal rabbit IgG or 2% heat inactivated normal rabbit serum for 30 minutes and use secondary rabbit antibody system at appropriate dilution with 100ug/ml of normal rabbit IgG. 2. Negative Control: Use another antigen affinity purified goat antibody at similar concentration to a protein that is not expressed on mouse cells as negative control.

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