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

234169
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      Aperçu

      Replacement Information

      Tableau de caractéristiques principal

      Species ReactivityHostAntibody Type
      H, M, R Rb Polyclonal Antibody

      Prix & Disponibilité

      Référence DisponibilitéConditionnement Qté Prix Quantité
      234169-500UL
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      Disponibilité limitéeDisponibilité limitée
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      Interrompu(e)
      Disponible en quantités limitées
      Disponibilité à confirmer
        Pour le restant : Nous vous tiendrons informé
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          Ampoule plast. 500 ul
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          Le prix n'a pas pu être récupéré
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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 Immunoprecipitation
          Frozen Sections
          Immunoblotting (Western Blotting)
          Immunofluorescence
          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

          Documentation

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

          Titre

          Fiche de données de sécurité des matériaux (FDS) 

          Anti-Collagen Type I/III, Cyanogen Bromide Fragments Rabbit pAb Certificats d'analyse

          TitreNuméro de lot
          234169

          Références bibliographiques

          Aperçu de la référence bibliographique
          Romanos, G.E., et al. 1992. J. Periodont. Res. 27, 101.
          Zimmermann, B., et al. 1992. Eur. Arch. Biol. 103, 93.
          Fiche technique

          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 ≤ -70°C
          Avoid freeze/thaw
          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.