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    products/secondary-antibodies/rabbit-syrian-hamster-igg-hl-biotin-ab6782.pdf

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Immunology Immunoglobulins Heavy Chain IgG
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Rabbit Anti-Syrian Hamster IgG H&L (Biotin) (ab6782)

  • Datasheet
  • SDS
Submit a review Q&A (3)References (6)

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Abpromise

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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Rabbit Anti-Syrian Hamster IgG H&L (Biotin) (ab6782)

    Key features and details

    • Rabbit Anti-Syrian Hamster 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

    HRP Texas Red ® Unconjugated

    こちらの製品もご検討ください

    標識
    Product image
    Streptavidin Conjugation Kit - Lightning-Link® (ab102921)
    ブロッキング
    Normal Rabbit Serum (ab166640)
    IHC
    Product image
    Streptavidin HRP (ready-to-use) (ab64269)

    関連製品

    医薬用外毒物

    製品の概要

    • 製品名

      Rabbit Anti-Syrian Hamster 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

      Syrian hamster
    • 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

      hamster 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

      Preservative: 0.01% Sodium azide
      Constituents: 1% BSA, 0.424% Potassium phosphate solution, 0.88% Sodium chloride
    • Concentration information loading...
    • 精製度

      Affinity purified
    • 特記事項(精製)

      Anti-Golden Syrian Hamster IgG Antibody was prepared from monospecific antiserum by immunoaffinity chromatography using Hamster IgG coupled to agarose.
    • 特記事項(標識)

      This product was prepared from monospecific antiserum by immunoaffinity chromatography using hamster IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities
    • ポリ/モノ

      ポリクローナル
    • 研究分野

      • Immunology
      • Immunoglobulins
      • Heavy Chain
      • IgG
      • Secondary antibodies
      • anti-Hamster
      • IgG
      • Biotin

    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ab6782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
    Use at an assay dependent concentration.
    ELISA
    1/20000 - 1/100000.
    IHC-P
    Use at an assay dependent concentration.
    IHC-Fr
    Use at an assay dependent concentration.
    Immunomicroscopy
    Use at an assay dependent concentration.
    ICC/IF
    1/1000 - 1/5000.
    WB
    Use at an assay dependent concentration.
    特記事項
    Dot blot
    Use at an assay dependent concentration.
    ELISA
    1/20000 - 1/100000.
    IHC-P
    Use at an assay dependent concentration.
    IHC-Fr
    Use at an assay dependent concentration.
    Immunomicroscopy
    Use at an assay dependent concentration.
    ICC/IF
    1/1000 - 1/5000.
    WB
    Use at an assay dependent concentration.

    画像

    • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Rabbit Anti-Syrian Hamster IgG H&L (Biotin) (ab6782)
      Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Rabbit Anti-Syrian Hamster IgG H&L (Biotin) (ab6782)
      Ab6782 was used at dilution 1/800 with the primary antibody ab11936 in IHC-P. See the review on ab11936.

    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

    データシートおよび資料

    • SDS download

    • Datasheet download

      Download

    参考文献 (6)

    ab6782 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。

    ab6782 は 6 報の論文で使用されています。

    • Zhang M  et al. LncRNA SNHG5 affects cell proliferation, metastasis and migration of colorectal cancer through regulating miR-132-3p/CREB5. Cancer Biol Ther 20:524-536 (2019). PubMed: 30395767
    • Lee D  et al. HMGB2 is a novel adipogenic factor that regulates ectopic fat infiltration in skeletal muscles. Sci Rep 8:9601 (2018). PubMed: 29942000
    • Liu J  et al. Downregulation of let-7b promotes COL1A1 and COL1A2 expression in dermis and skin fibroblasts during heat wound repair. Mol Med Rep 13:2683-8 (2016). PubMed: 26861712
    • Alymova IV  et al. A novel cytotoxic sequence contributes to influenza A viral protein PB1-F2 pathogenicity and predisposition to secondary bacterial infection. J Virol 88:503-15 (2014). PubMed: 24173220
    • Guo Q  et al. Mouse lymphatic endothelial cell targeted probes: anti-LYVE-1 antibody-based magnetic nanoparticles. Int J Nanomedicine 8:2273-84 (2013). IHC-P . PubMed: 23818783
    • Barnes NL  et al. Cyclooxygenase-2 inhibition: effects on tumour growth, cell cycling and lymphangiogenesis in a xenograft model of breast cancer. Br J Cancer 96:575-82 (2007). PubMed: 17285134

    レビューと Q&A

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    レビューを送る 質問を送る

    1-3 of 3 Abreviews or Q&A

    Question

    Following our standard protocol for IHC, I could not detect specific staining for CD11c in spleen and ear (dermis) sections. A staining with anti MHC II that I performed in parallel worked just fine. Could you please suggest me how to improve my protocol? According to a paper stated in your bibliography, Metlay 1990 J. Exp. Med. 171:1753, I used acetone for fixation. 1. Take (cryo-)sections out the freezer and warm at RT for 30` 2. Fixation: in cuvette with ice-cold acetone 10` 3. Permeabilization and washing: 3 x 5` in PBS at RT, 1st wash with 0.2%TX-100 4. Blocking: 30` with 5% goat serum in PBS (500µl/slide) 5. 1st antibody: in 5% goat serum O/N, 4ºC (200µl/slide + parafilm) I used up to 1:50 dilution for the hamster anti-CD11c (20ng/ul), I controled the staining with sections, that did not receive 1st antibody. Also 1: 10,000 DAPI 6. Washing: 3 x 10` with PBS 7. 2nd antibody: in 2% goat serum O/N, 4ºC (200µl/slide + parafilm), I used your BIOTIN-anti Hamster 1:200 (5ng/ul) 8. Washing: 3 x 10` with PBS 9. ST-TRITC: in 2% goat serum O/N, 4ºC (200µl/slide + parafilm), I used a standard concentration of 1:200, that works well in other stainings 10. Washing: 2 x 10` in PBS 1 x 10` in Tris-HCl, pH 7.4 (remove salt) 11. Mounting: dry slides for a few minutes, Mowiol, store in dark at 4ºC I would be happpy to receive any suggestions,

    Read More

    Abcam community

    Verified customer

    Asked on Sep 01 2006

    Answer

    I apologise for the delay in responding to you, I have at last received feedback from the laboratory that tested ab33483 and include their response below: I have had a look through your customers protocol and note that it differs somewhat from our recommended protocol for cryostat sections. So firstly from their protocols: 1. I note sections appear to be stored in a freezer prior to staining. Some antigens are more sensitive to this than others, this may be the case here. I would recommend using freshly sectioned material 2. Following acetone fixation they have included a triton step (for the DAPI?). This may not be compatible with staining for CD11c using this antibody. I would suggest omitting this step. I note from the literature that such a step is not included in publications reporting successful staining with this antibody. 3. We do not support the use of Immunofluorescence for this antibody. I do not know whether there is sufficient sensitivity to allow the use of TRIT-C for its detection. I would suggest the use of a peroxidase-DAB protocol as has been used in all the publication reporting successful. My gut feeling is that it may be the Triton X-100 that may affect the epitope recognised by the antibody. Just omitting this step may help restore antigenicity. Please find a list of publications where this has been used successfully for IHC on cryostat sections. There may be further appropriate advice in these. 1: Witmer-Pack MD, Crowley MT, Inaba K, Steinman RM. Macrophages, but not dendritic cells, accumulate colloidal carbon following administration in situ. J Cell Sci. 1993 Aug;105 ( Pt 4):965-73. PMID: 7693737 2: Metlay JP, Witmer-Pack MD, Agger R, Crowley MT, Lawless D, Steinman RM. The distinct leukocyte integrins of mouse spleen dendritic cells as identified with new hamster monoclonal antibodies. J Exp Med. 1990 May 1;171(5):1753-71. PMID: 2185332 3: McMenamin PG. Dendritic cells and macrophages in the uveal tract of the normal mouse eye. Br J Ophthalmol. 1999 May;83(5):598-604. PMID: 10216062 4: Pimorady-Esfahani A, Grounds MD, McMenamin PG. Macrophages and dendritic cells in normal and regenerating murine skeletal muscle. Muscle Nerve. 1997 Feb;20(2):158-66. PMID: 9040653 5: Kelsall BL, Strober W. Distinct populations of dendritic cells are present in the subepithelial dome and T cell regions of the murine Peyer's patch. J Exp Med. 1996 Jan 1;183(1):237-47. PMID: 8551227 6: Dahlen E, Dawe K, Ohlsson L, Hedlund G. Dendritic cells and macrophages are the first and major producers of TNF-alpha in pancreatic islets in the nonobese diabetic mouse. J Immunol. 1998 Apr 1;160(7):3585-93. PMID: 9531322 7: Leenen PJ, Radosevic K, Voerman JS, Salomon B, van Rooijen N, Klatzmann D, van Ewijk W. Heterogeneity of mouse spleen dendritic cells: in vivo phagocytic activity, expression of macrophage markers, and subpopulation turnover. J Immunol. 1998 Mar 1;160(5):2166-73. PMID: 9498754 8: Gonzalez-Juarrero M, Orme IM. Characterization of murine lung dendritic cells infected with Mycobacterium tuberculosis. Infect Immun. 2001 Feb;69(2):1127-33. PMID: 11160010 9: Hamada H, Hiroi T, Nishiyama Y, Takahashi H, Masunaga Y, Hachimura S, Kaminogawa S, Takahashi-Iwanaga H, Iwanaga T, Kiyono H, Yamamoto H, Ishikawa H. Identification of multiple isolated lymphoid follicles on the antimesenteric wall of the mouse small intestine. J Immunol. 2002 Jan 1;168(1):57-64. PMID: 11751946 10: Bjorck P. Dendritic cells exposed to herpes simplex virus in vivo do not produce IFN-alpha after rechallenge with virus in vitro and exhibit decreased T cell alloreactivity. J Immunol. 2004 May 1;172(9):5396-404. PMID: 15100280 Please note that most of these appear to be available freely via PubMed. Reference 1 has some great pictures of staining in the liver and in spleen with N418 and other antibodies such as F4/80 and FA-11 etc. I hope this advice will be useful. Please do not hesitate to contact me if you still experience problems with those recommendations, if you purchased the antibody in the last 90 days I would be happy to offer you a refund,

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    Abcam Scientific Support

    Answered on Sep 18 2006

    Question

    I found this information on the web: http://www.histosearch.com/histonet/Oct04/Re.HistonetBackgroundwithC.html where it is recommended to pre-absorb the secondary detecting a hamster monoclonal to CD11c. I bought both antibodies from you, please advise on how to use the secondary. Thanks

    Read More

    Abcam community

    Verified customer

    Asked on Aug 30 2006

    Answer

    Thank you for your enquiry. The protocol quoted in the link you kindly provided does not seem to mention our antibodies but antibodies from other companies. In our experience the secondary ab6782 does not give background problems and does not need to be pre-absorbed. If you experience any problems or need further advice regarding your IHC protocol please do not hesitate to contact me, I would be happy to look at your full protocol,

    Read More

    Abcam Scientific Support

    Answered on Aug 31 2006

    Question

    Is this Ab appropriate as a labeling secondary Ab (for IHC) to an Armenian hamster IgG, group 3, lamda (anti-mouse CD51 monoclonal antibody)

    Read More

    Abcam community

    Verified customer

    Asked on Jul 09 2001

    Answer

    This antibody is not recommended for Armenian hamster IgG.

    Read More

    Neil Hayward

    Abcam Scientific Support

    Answered on Jul 10 2001

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
    For licensing inquiries, please contact partnerships@abcam.com

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