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281751 DAB, Tetrahydrochloride, 50X Concentrate

This DAB, Tetrahydrochloride, 50X Concentrate is validated for use in Immunoblotting, Immunohistochemistry.

DAB, Tetrahydrochloride, 50X Concentrate: のSDS（安全データシート）、CoA（試験成績書）およびCoQ（品質証明書）、カタログなど製品関連の技術資料を入手いただけます。

同義語: 3,3ʹ-Diaminobenzidine

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281751
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概要

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281751-10MLCN
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      		 ｶﾞﾗｽﾋﾞﾝ 10 ml
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      Description
      OverviewProduces a brown alcohol-insoluble end product. Also useful as a stain for myelin in glutaraldehyde-fixed sections. Supplied as a 50X concentrate.
      Catalogue Number281751
      Brand Family Calbiochem®
      Synonyms3,3ʹ-Diaminobenzidine
      References
      ReferencesKrueger, S.K., et al. 1999. Biotech. Histochem. 74, 105.
      Larrson, L.I. 1988. Immunocytochemistry: Theory and Practice, CRC Press, Inc., Boca Raton, FL.
      Gallyas, F., et al. 1982. J. Histochem. Cytochem. 30, 183.
      Hsu, S.M. and Soban, E. 1982. J. Histochem. Cytochem. 30, 1079.
      Lewis, P.R. and Knight, D.P. 1977. Staining Methods for Sectioned Material, In Practical Methods in Electron Microscopy, A.M. Glauert, ed. North-Holland, Amsterdam.
      Graham, R.C., Jr. and Karnovsky, M.J. 1966. J. Histochem. Cytochem. 14, 291.
      Product Information
      CAS number7411-49-6
      FormBrown to dark brown solution
      FormulationSupplied as a 50X concentrate.
      PreservativeNone
      Quality LevelMQ100
      Applications
      Application NotesImmunoblotting (see comments)
      Immunohistochemistry (see comments)
      Application CommentsStable at 4°C and 18-26°C.

      Suggested Procedure for Immunohistochemical Staining Using DAB:

      1. Complete all required incubations with antibodies and HRP-labeled probes, and all necessary wash steps.
      2. Prepare 1X DAB Substrate Buffer: Add 9 parts distilled water to 1 part 10X DAB Substrate Buffer (Cat. No. 281753). Mix well. [Note: 1 M Tris-HCl, pH 7.6 may be substituted for Cat. No. 281753, such that the final (1X) concentration is 100 mM Tris-HCl, pH 7.6.
      3. Prepare 1X DAB Substrate Solution: Add 1 part 50X DAB Concentrate and 1 part 0.5% H2O2 to 50 parts 1X DAB Substrate Buffer (prepared in Step 2). Mix well and protect from light.
      4. Following the final wash, completely cover tissue sections with the 1X DAB Substrate Solution (prepared in Step 3) and incubate 5-15 min at room temperature. Note: Variables associated with assay conditions will dictate the proper reaction time.
      5. After reaction is complete, wash tissue sections thoroughly in distilled water.
      6. Counterstain with hematoxylin if desired.
      7. Dehydrate in graded alcohols, xylene, or xylene substitutes.
      8. Mount tissue sections using xylene-based mounting media.

      Suggested Procedure for Immunoblot Staining with DAB:

      1. Complete all required incubations with antibodies and HRP-labeled probes, and all necessary wash steps.
      2. Prepare 1X DAB Substrate Buffer: Add 9 parts distilled water to 1 part 10X DAB Substrate Buffer (Cat. No. 281753). Mix well. [Note: 1 M Tris-HCl, pH 7.6 may be substituted for Cat. No. 281753, such that the final (1X) concentration is 100 mM Tris-HCl, pH 7.6.]
      3. Prepare 1X DAB Substrate Solution: Add 1 part 50X DAB Concentrate and 1 part 0.5% H2O2 to 50 parts 1X DAB Substrate Buffer (prepared in Step 2). Mix well and protect from light.
      4. Following the final wash, completely cover membranes with 1X DAB Substrate Solution (prepared in Step 3). Incubate 5-30 min at room temperature.
      Note: Variables associated with assay conditions will dictate the proper reaction time.
      5. After reaction is complete, wash membranes thoroughly in distilled water.
      6. Air-dry membranes and store protected from light.
      Biological Information
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      RTECSDV8753000
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Toxic
      Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping charges may be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
      Storage +2°C to +8°C
      Do not freeze Ok to freeze
      Special InstructionsDiscard if a precipitate forms or if reagent is purple (the purple material is a DAB oxidation product that binds avidly to heme-containing proteins).
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      281751-10MLCN 04055977197808

      Documentation

      DAB, Tetrahydrochloride, 50X Concentrate (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      DAB, Tetrahydrochloride, 50X Concentrate 試験成績書（CoA）

      タイトルロット番号
      281751

      参考資料

      参考資料の概要
      Krueger, S.K., et al. 1999. Biotech. Histochem. 74, 105.
      Larrson, L.I. 1988. Immunocytochemistry: Theory and Practice, CRC Press, Inc., Boca Raton, FL.
      Gallyas, F., et al. 1982. J. Histochem. Cytochem. 30, 183.
      Hsu, S.M. and Soban, E. 1982. J. Histochem. Cytochem. 30, 1079.
      Lewis, P.R. and Knight, D.P. 1977. Staining Methods for Sectioned Material, In Practical Methods in Electron Microscopy, A.M. Glauert, ed. North-Holland, Amsterdam.
      Graham, R.C., Jr. and Karnovsky, M.J. 1966. J. Histochem. Cytochem. 14, 291.
      データシート

      Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

      Revision21-August-2007 JSW
      Synonyms3,3ʹ-Diaminobenzidine
      ApplicationImmunoblotting (see comments)
      Immunohistochemistry (see comments)
      DescriptionPeroxidase substrate that forms an insoluble, brown precipiate. Supplied as a 50X concentrate. Designed for use with DAB Substrate Buffer (Cat. No. 281753).
      BackgroundSince first introduced by Graham and Karnovsky numerous procedures for the use of DAB for detection of horseradish peroxidase (HRP)-labeled probes in histochemistry, immunohistochemistry, western blots and dot blots have been described. In the presence of horseradish peroxidase and hydrogen peroxide, DAB is oxidized to a brown polymer that is insoluble in most organic solvents. Thus, xylene-based mounting media may be used for immunohistochemical applications. Sites of HRP activity on tissue sections and blots appear as brown-orange deposits. The color can be modified and intensified by treatment with salts of silver, copper, nickel, cobalt and osmium. This DAB substrate preparation is a stable, convenient, liquid concentrate in a proprietary solvent. The stabilization system prevents formation of partially oxidized DAB, thus eliminating the nonspecific binding to other heme-containing proteins so often observed with powdered DAB preparations. The concentrate can be diluted in appropriate peroxide-containing buffers, providing the researcher with the capability of formulating any of the numerous published DAB reaction systems.
      FormBrown to dark brown solution
      FormulationSupplied as a 50X concentrate.
      CAS number7411-49-6
      RTECSDV8753000
      PreservativeNone
      CommentsStable at 4°C and 18-26°C.

      Suggested Procedure for Immunohistochemical Staining Using DAB:

      1. Complete all required incubations with antibodies and HRP-labeled probes, and all necessary wash steps.
      2. Prepare 1X DAB Substrate Buffer: Add 9 parts distilled water to 1 part 10X DAB Substrate Buffer (Cat. No. 281753). Mix well. [Note: 1 M Tris-HCl, pH 7.6 may be substituted for Cat. No. 281753, such that the final (1X) concentration is 100 mM Tris-HCl, pH 7.6.
      3. Prepare 1X DAB Substrate Solution: Add 1 part 50X DAB Concentrate and 1 part 0.5% H2O2 to 50 parts 1X DAB Substrate Buffer (prepared in Step 2). Mix well and protect from light.
      4. Following the final wash, completely cover tissue sections with the 1X DAB Substrate Solution (prepared in Step 3) and incubate 5-15 min at room temperature. Note: Variables associated with assay conditions will dictate the proper reaction time.
      5. After reaction is complete, wash tissue sections thoroughly in distilled water.
      6. Counterstain with hematoxylin if desired.
      7. Dehydrate in graded alcohols, xylene, or xylene substitutes.
      8. Mount tissue sections using xylene-based mounting media.

      Suggested Procedure for Immunoblot Staining with DAB:

      1. Complete all required incubations with antibodies and HRP-labeled probes, and all necessary wash steps.
      2. Prepare 1X DAB Substrate Buffer: Add 9 parts distilled water to 1 part 10X DAB Substrate Buffer (Cat. No. 281753). Mix well. [Note: 1 M Tris-HCl, pH 7.6 may be substituted for Cat. No. 281753, such that the final (1X) concentration is 100 mM Tris-HCl, pH 7.6.]
      3. Prepare 1X DAB Substrate Solution: Add 1 part 50X DAB Concentrate and 1 part 0.5% H2O2 to 50 parts 1X DAB Substrate Buffer (prepared in Step 2). Mix well and protect from light.
      4. Following the final wash, completely cover membranes with 1X DAB Substrate Solution (prepared in Step 3). Incubate 5-30 min at room temperature.
      Note: Variables associated with assay conditions will dictate the proper reaction time.
      5. After reaction is complete, wash membranes thoroughly in distilled water.
      6. Air-dry membranes and store protected from light.
      Storage +2°C to +8°C
      Do Not Freeze Ok to freeze
      Special InstructionsDiscard if a precipitate forms or if reagent is purple (the purple material is a DAB oxidation product that binds avidly to heme-containing proteins).
      Toxicity Toxic
      ReferencesKrueger, S.K., et al. 1999. Biotech. Histochem. 74, 105.
      Larrson, L.I. 1988. Immunocytochemistry: Theory and Practice, CRC Press, Inc., Boca Raton, FL.
      Gallyas, F., et al. 1982. J. Histochem. Cytochem. 30, 183.
      Hsu, S.M. and Soban, E. 1982. J. Histochem. Cytochem. 30, 1079.
      Lewis, P.R. and Knight, D.P. 1977. Staining Methods for Sectioned Material, In Practical Methods in Electron Microscopy, A.M. Glauert, ed. North-Holland, Amsterdam.
      Graham, R.C., Jr. and Karnovsky, M.J. 1966. J. Histochem. Cytochem. 14, 291.