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234169 Anti-Collagen Type I/III, Cyanogen Bromide Fragments Rabbit pAb

Anti-Collagen Type I/III, Cyanogen Bromide Fragments, rabbit polyclonal specifically recognizes type I and III collagens. It is validated for WB, IF, IP, and IHC with frozen sections.

Anti-Collagen Type I/III, Cyanogen Bromide Fragments Rabbit pAb: 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。
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234169
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概要

Replacement Information

主要スペック表

Species ReactivityHostAntibody Type
H, M, RRbPolyclonal Antibody

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      Description
      OverviewRecognizes type I and type III collagens. Does not cross-react with fibronectin or type II, type V, or type VI collagen.
      Catalogue Number234169
      Brand Family Calbiochem®
      References
      ReferencesRomanos, G.E., et al. 1992. J. Periodont. Res. 27, 101.
      Zimmermann, B., et al. 1992. Eur. Arch. Biol. 103, 93.
      Product Information
      FormLiquid
      FormulationUndiluted serum.
      PreservativeNone
      Quality LevelMQ100
      Applications
      Key Applications Frozen Sections
      Immunoblotting (Western Blotting)
      Immunofluorescence
      Immunoprecipitation
      Application NotesFrozen Sections (1:30-1:60, see comments)
      Immunoblotting (1:200-1:500)
      Immunofluorescence (1:20-1:40)
      Immunoprecipitation (1:20-1:60)
      Application CommentsFor frozen sections, enzymatic or heat (41°C) pretreatment is recommended to unwind the triple helical structure. Does not cross-react with type II, type V, or type VI collagen. Variables associated with assay conditions will dictate the proper working dilution.

      This protocol is provided only as a general guide. Researchers should standardize this assay for their own specific needs and should consult published literature.

      Immunohistochemistry Protocol

      Introduction

      Staining of cryosections using anti-collagen antibodies requires either heat and/or enzymatic treatment in order to unwind the triple helical structure of collagen. An initial heat treatment aids in unwinding the collagen, while maintaining the antigen structure. Subsequent enzymatic treatment with hyaluronidase facilitates the removal of macromolecules that further hinder recognition by the antibody. In some cases it is also necessary to perform a second enzymatic digestion using chondroitinase ABC.

      Protocol

      Reagents and Equipment:

      • Cryostat sections of desired tissue: cut into 5 mm sections and place on clean glass slides treated with poly-L-lysine
      • PBS (phosphate buffered saline): dissolve 8 g NaCl, 200 mg KCl, 1.44 g Na2HPO4, and 240 mg KH2PO4 in 800 ml dH2O; adjust the pH to 7.4 with HCl; add dH2O to 1 L
      • PBS/BSA (phosphate buffered saline/bovine serum albumin): 0.5% BSA prepared in PBS
      • Testicular hyaluronidase: 2 mg/ml in cold PBS
      • Chondroitinase ABC: 2 mg/ml in PBS
      • Normal sheep serum
      • Primary antibody: Anti-Collagen, Type I/III, Cyanogen Bromide Fragments Rabbit pAb (Cat. No. 234169); diluted as recommended
      • Secondary antibody: goat anti-rabbit IgG, fluorescein conjugated
      • p-Phenylenediamine: 0.1% in glycerin:PBS (9:1)
      • Staining chamber
      • Wet chamber for incubations: chamber in which a small amount of PBS or dH2O is added to maintain a humid environment; slides should not be submerged

      Protocol:

      • Prepare 5 µm cryostat tissue sections from the tissue of choice and place on clean glass slides that have been treated with poly-L-lysine.
      • Incubate the tissue sections in a staining chamber with 0.5% BSA/PBS for 5-10 min at 41°-43°C. This serves to block the sections and unwind the helical structure.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • Treat the sections with 10 µl of hyaluronidase stock (2 mg/ml) by applying the enzyme directly to the sections on the slide. If 10 µl does not completely cover the section, increase the volume of enzyme until the section is completely covered. Incubate in a wet chamber at room temperature for 30 min. Stop the reaction by treatment of the sections with 25-50 µl of normal sheep serum.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • If desired, a second enzymatic treatment can be carried out by treating the sections with 10 µl of chondroitinase ABC (2 mg/ml); apply directly to the sections as above. If 10 µl does not completely cover the section, increase the volume of enzyme until the section is completely covered. Incubate in a wet chamber at room temperature for 30 min. Stop the reaction by treatment of the sections with 25-50 µl of normal sheep serum.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • Apply 5-10 µl of primary antibody (diluted to the desired concentration) to the section and incubate in a wet chamber at 37°C for 45 min.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • Apply 5-10 µl of secondary antibody (diluted to the desired concentration) to the section and incubate in a wet chamber at 37°C for 1 h. Protect from light during the incubation.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS in a staining chamber. Carefully remove excess fluid, but do not allow the slides to completely dry, as the secondary antibody may form crystals.
      • Place 1 drop of 0.1% p-phenylenediamine on the section and mount under a coverslip. The slides can be stored at 4°C up to 2 days.
      • Fixation:
      The best results have been obtained on cryosections without fixation. The risk of collagen loss is relatively low, as its solubility in neutral buffer is negligible. However, other antigens may diffuse into the incubation medium and settle along adjacent tissue structures or form diffusion artifacts. If fixation is necessary, dehydration with ethanol or acetone at -20°C for 5-10 min is recommended. Fixation should take place following enzymatic treatment (step 5). Aldehyde (formaldehyde or glutaraldehyde) fixation is NOT recommended. If aldehyde fixation cannot be avoided, do not exceed 2% of the fixative (less than 1% is recommended).

      Notes:

      • It may not be necessary to treat the sections with both heat and hyaluronidase and/or chondroitinase ABC. It is recommended that heat treatment be used initially and, if further epitope exposure is necessary, then treat with hyaluronidase. Chondroitinase ABC treatment is usually not necessary.
      • If hyaluronidase and chondroitinase ABC are both desired, it is recommended that the digestions be carried out separately.
      Biological Information
      Immunogenpurified, fetal mouse skin collagens type I and III, digested with cyanogen bromide
      ImmunogenFetal Mouse Skin
      HostRabbit
      IsotypeIgG
      Species Reactivity
      • Human
      • Mouse
      • Rat
      Antibody TypePolyclonal Antibody
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Dry Ice Only
      Toxicity Standard Handling
      Storage ≤ -70°C
      Avoid freeze/thaw Avoid freeze/thaw
      Do not freeze Ok to freeze
      Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      234169-500ULCN 04055977200089

      Documentation

      Anti-Collagen Type I/III, Cyanogen Bromide Fragments Rabbit pAb (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      Anti-Collagen Type I/III, Cyanogen Bromide Fragments Rabbit pAb 試験成績書（CoA）

      タイトルロット番号
      234169

      参考資料

      参考資料の概要
      Romanos, G.E., et al. 1992. J. Periodont. Res. 27, 101.
      Zimmermann, B., et al. 1992. Eur. Arch. Biol. 103, 93.
      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.

      Revision26-July-2007 RFH
      ApplicationFrozen Sections (1:30-1:60, see comments)
      Immunoblotting (1:200-1:500)
      Immunofluorescence (1:20-1:40)
      Immunoprecipitation (1:20-1:60)
      DescriptionRabbit polyclonal antibody supplied as undiluted serum. Recognizes type I and type III collagen.
      BackgroundCollagens are major fibrous structural elements of cartilage, tendon, bone, skin, lung, and blood vessels. Type I collagen, a heterotrimer consisting of two α1(I) chains and one α2(I) chain, is the most abundant fibrillar collagen. Type I collagen is primarily found in bone, tendon and skin. Type III collagen consists of three α1(III) chains, and is most often found in skin, blood vessels, and internal organs.
      HostRabbit
      Immunogen speciesFetal Mouse Skin
      Immunogenpurified, fetal mouse skin collagens type I and III, digested with cyanogen bromide
      IsotypeIgG
      Specieshuman, mouse, rat
      FormLiquid
      FormulationUndiluted serum.
      PreservativeNone
      CommentsFor frozen sections, enzymatic or heat (41°C) pretreatment is recommended to unwind the triple helical structure. Does not cross-react with type II, type V, or type VI collagen. Variables associated with assay conditions will dictate the proper working dilution.

      This protocol is provided only as a general guide. Researchers should standardize this assay for their own specific needs and should consult published literature.

      Immunohistochemistry Protocol

      Introduction

      Staining of cryosections using anti-collagen antibodies requires either heat and/or enzymatic treatment in order to unwind the triple helical structure of collagen. An initial heat treatment aids in unwinding the collagen, while maintaining the antigen structure. Subsequent enzymatic treatment with hyaluronidase facilitates the removal of macromolecules that further hinder recognition by the antibody. In some cases it is also necessary to perform a second enzymatic digestion using chondroitinase ABC.

      Protocol

      Reagents and Equipment:

      • Cryostat sections of desired tissue: cut into 5 mm sections and place on clean glass slides treated with poly-L-lysine
      • PBS (phosphate buffered saline): dissolve 8 g NaCl, 200 mg KCl, 1.44 g Na2HPO4, and 240 mg KH2PO4 in 800 ml dH2O; adjust the pH to 7.4 with HCl; add dH2O to 1 L
      • PBS/BSA (phosphate buffered saline/bovine serum albumin): 0.5% BSA prepared in PBS
      • Testicular hyaluronidase: 2 mg/ml in cold PBS
      • Chondroitinase ABC: 2 mg/ml in PBS
      • Normal sheep serum
      • Primary antibody: Anti-Collagen, Type I/III, Cyanogen Bromide Fragments Rabbit pAb (Cat. No. 234169); diluted as recommended
      • Secondary antibody: goat anti-rabbit IgG, fluorescein conjugated
      • p-Phenylenediamine: 0.1% in glycerin:PBS (9:1)
      • Staining chamber
      • Wet chamber for incubations: chamber in which a small amount of PBS or dH2O is added to maintain a humid environment; slides should not be submerged

      Protocol:

      • Prepare 5 µm cryostat tissue sections from the tissue of choice and place on clean glass slides that have been treated with poly-L-lysine.
      • Incubate the tissue sections in a staining chamber with 0.5% BSA/PBS for 5-10 min at 41°-43°C. This serves to block the sections and unwind the helical structure.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • Treat the sections with 10 µl of hyaluronidase stock (2 mg/ml) by applying the enzyme directly to the sections on the slide. If 10 µl does not completely cover the section, increase the volume of enzyme until the section is completely covered. Incubate in a wet chamber at room temperature for 30 min. Stop the reaction by treatment of the sections with 25-50 µl of normal sheep serum.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • If desired, a second enzymatic treatment can be carried out by treating the sections with 10 µl of chondroitinase ABC (2 mg/ml); apply directly to the sections as above. If 10 µl does not completely cover the section, increase the volume of enzyme until the section is completely covered. Incubate in a wet chamber at room temperature for 30 min. Stop the reaction by treatment of the sections with 25-50 µl of normal sheep serum.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • Apply 5-10 µl of primary antibody (diluted to the desired concentration) to the section and incubate in a wet chamber at 37°C for 45 min.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS. Carefully remove excess fluid and air-dry the slides.
      • Apply 5-10 µl of secondary antibody (diluted to the desired concentration) to the section and incubate in a wet chamber at 37°C for 1 h. Protect from light during the incubation.
      • Carefully rinse by briefly submerging in PBS.
      • Wash 2 x 10 min in PBS in a staining chamber. Carefully remove excess fluid, but do not allow the slides to completely dry, as the secondary antibody may form crystals.
      • Place 1 drop of 0.1% p-phenylenediamine on the section and mount under a coverslip. The slides can be stored at 4°C up to 2 days.
      • Fixation:
      The best results have been obtained on cryosections without fixation. The risk of collagen loss is relatively low, as its solubility in neutral buffer is negligible. However, other antigens may diffuse into the incubation medium and settle along adjacent tissue structures or form diffusion artifacts. If fixation is necessary, dehydration with ethanol or acetone at -20°C for 5-10 min is recommended. Fixation should take place following enzymatic treatment (step 5). Aldehyde (formaldehyde or glutaraldehyde) fixation is NOT recommended. If aldehyde fixation cannot be avoided, do not exceed 2% of the fixative (less than 1% is recommended).

      Notes:

      • It may not be necessary to treat the sections with both heat and hyaluronidase and/or chondroitinase ABC. It is recommended that heat treatment be used initially and, if further epitope exposure is necessary, then treat with hyaluronidase. Chondroitinase ABC treatment is usually not necessary.
      • If hyaluronidase and chondroitinase ABC are both desired, it is recommended that the digestions be carried out separately.
      Storage Avoid freeze/thaw
      ≤ -70°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing initial thaw, aliquot and freeze (-70°C).
      Toxicity Standard Handling
      ReferencesRomanos, G.E., et al. 1992. J. Periodont. Res. 27, 101.
      Zimmermann, B., et al. 1992. Eur. Arch. Biol. 103, 93.