NE1023 Anti-Neurofilament H Non-Phosphorylated Mouse mAb (SMI-32)

NE1023
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      Overview

      Replacement Information

      Key Specifications Table

      Species ReactivityHostAntibody Type
      Ma M Monoclonal Antibody

      Pricing & Availability

      Catalog Number AvailabilityPackaging Qty/Pack Price Quantity
      NE1023-100UL
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          Plastic ampoule 100 ul
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          Description
          Overview

          This product has been discontinued.



          We are offering Anti-Neurofilament H Non-Phosphorylated Mouse MAb (SMI-32) (Cat. No. 559844) as a possible alternative. Please read the alternative product documentation carefully and contact technical service if you need additional information.






          Recognizes the non-phosphorylated ~180 kDa-200 kDa neurofilament H protein in rat central nervous system (CNS) cytoskeletal preparations.

          Catalogue NumberNE1023
          Brand Family Calbiochem®
          Application Data
          Detection of non-phosphorylated rat neurofilament H by staining frozen sections. Sample: Rat brain. Primary antibody: Anti-Neurofilament H Non-Phosphorylated Mouse mAb (SMI-32) (Cat. No. NE1023) (1:1000). Detection: fluorescence (green) with Hoechst 33342 counterstain.
          References
          ReferencesTrapp, B.D., et al. 1998. N. Engl. J. Med. 338, 278.
          King, C.E., et al. 1997. Neuroreport. 8, 1663.
          Campbell, M.J., et al. 1991. Brain Res. 539, 133.
          Campbell, M.J., et al. 1989. J. Comp. Neurol. 282, 191.
          Sternberger, L.A., et al. 1983. Proc. Natl. Acad. Sci. USA 80, 6126.
          Product Information
          FormLiquid
          FormulationUndiluted ascites.
          Positive controlRat brain or central nervous system cytoskeletal preparations
          Preservative≤0.1% sodium azide
          Applications
          Key Applications Immunocytochemistry
          Paraffin Sections
          Enzyme-Linked Immunosorbent Assay
          Frozen Sections
          Immunoblotting (Western Blotting)
          Application NotesELISA (1:1000)
          Frozen Sections (1:1000, see comments)
          Immunoblotting (1:1000, see comments)
          Immunocytochemistry (1:1000, see comments)
          Paraffin Sections (1:1000, heat pre-treatment required, see comments)
          Application CommentsOnly recognizes non-phosphorylated neurofilament H. By immunocytochemistry this antibody stains neuronal cell bodies, dendrites, and some thick axons in the central and peripheral nervous systems, but does not stain thin axons or other cells and tissues. Tissues and cultured cells can be fixed in a variety of paraformaldehyde- or formaldehye-containing fixatives, such as Bouin's fixative. Antibody reactivity is poor in glutaraldehyde/paraformaldehyde-fixed samples. For staining formalin-fixed, paraffin sections it is recommended that de-paraffinized tissue be autoclaved in dH2O for 10 min or boiled in Tris-buffered saline, pH 9.0, in a microwave for 15 min. Trypsin pre-treatment abolishes antibody binding to the epitope. Post-fixation in cold methanol or methanol/hydrogen peroxide facilitates access of the antibody to the neurons in frozen sections or thick sections fixed in 4% paraformaldehyde and in cultured cells. By immunoblotting this antibody detects two bands, ~180 and ~200 kDa, which merge into a single NFH line on two-dimensional gels. Antibody should be titrated for optimal results in individual systems.
          Biological Information
          Immunogenhomogenized hypothalami from Fischer 344 rat brain
          ImmunogenRat
          CloneSMI-32
          HostMouse
          IsotypeIgG₁
          Species Reactivity
          • Mammals
          Antibody TypeMonoclonal Antibody
          Physicochemical Information
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          Safety Information
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Blue Ice Only
          Toxicity Standard Handling
          Storage +2°C to +8°C
          Avoid freeze/thaw Avoid freeze/thaw
          Do not freeze Ok to freeze
          Special InstructionsFollowing initial thaw, aliquot and freeze (-20°C).
          Packaging Information
          Transport Information
          Supplemental Information
          Specifications

          Documentation

          Anti-Neurofilament H Non-Phosphorylated Mouse mAb (SMI-32) SDS

          Title

          Safety Data Sheet (SDS) 

          Anti-Neurofilament H Non-Phosphorylated Mouse mAb (SMI-32) Certificates of Analysis

          TitleLot Number
          NE1023

          References

          Reference overview
          Trapp, B.D., et al. 1998. N. Engl. J. Med. 338, 278.
          King, C.E., et al. 1997. Neuroreport. 8, 1663.
          Campbell, M.J., et al. 1991. Brain Res. 539, 133.
          Campbell, M.J., et al. 1989. J. Comp. Neurol. 282, 191.
          Sternberger, L.A., et al. 1983. Proc. Natl. Acad. Sci. USA 80, 6126.
          Data Sheet

          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.

          Revision01-October-2007 RFH
          ApplicationELISA (1:1000)
          Frozen Sections (1:1000, see comments)
          Immunoblotting (1:1000, see comments)
          Immunocytochemistry (1:1000, see comments)
          Paraffin Sections (1:1000, heat pre-treatment required, see comments)
          Application Data
          Detection of non-phosphorylated rat neurofilament H by staining frozen sections. Sample: Rat brain. Primary antibody: Anti-Neurofilament H Non-Phosphorylated Mouse mAb (SMI-32) (Cat. No. NE1023) (1:1000). Detection: fluorescence (green) with Hoechst 33342 counterstain.
          DescriptionMouse monoclonal antibody supplied as undiluted ascites. Recognizes the ~180-200 kDa non-phosphorylated neurofilament H protein.
          BackgroundNeurofilaments are a type of intermediate filament that serve as major constituent of the cytoskeleton of axons. They are the most abundant fibrillar components of the axon and are composed of three intertwined protofibrils. The neurofilament triplet proteins (NF-L, 68/70 kDa; NF-M, 160 kDa; and NF-H, 200 kDa) are found in both the central and peripheral nervous system and are usually neuron-specific. NF-H and NF-M both require the presence of NF-L protein to co-assemble. NF-H and NF-M become highly phosphorylated after newly formed neurofilaments enter the axon. Neurofilament staining is observed in neuromas, ganglioneuromas, gangliogliomas, ganglioneuroblastomas and neuroblastomas, and have also been detected in paragangliomas and adrenal and extra-adrenal pheochromocytomas. Carcinoids, neuroendocrine carcinomas of the skin, and oat cell carcinomas of the lung are also known to express neurofilaments.
          HostMouse
          Immunogen speciesRat
          Immunogenhomogenized hypothalami from Fischer 344 rat brain
          CloneSMI-32
          IsotypeIgG₁
          Speciesmammalian
          Positive controlRat brain or central nervous system cytoskeletal preparations
          FormLiquid
          FormulationUndiluted ascites.
          Preservative≤0.1% sodium azide
          CommentsOnly recognizes non-phosphorylated neurofilament H. By immunocytochemistry this antibody stains neuronal cell bodies, dendrites, and some thick axons in the central and peripheral nervous systems, but does not stain thin axons or other cells and tissues. Tissues and cultured cells can be fixed in a variety of paraformaldehyde- or formaldehye-containing fixatives, such as Bouin's fixative. Antibody reactivity is poor in glutaraldehyde/paraformaldehyde-fixed samples. For staining formalin-fixed, paraffin sections it is recommended that de-paraffinized tissue be autoclaved in dH2O for 10 min or boiled in Tris-buffered saline, pH 9.0, in a microwave for 15 min. Trypsin pre-treatment abolishes antibody binding to the epitope. Post-fixation in cold methanol or methanol/hydrogen peroxide facilitates access of the antibody to the neurons in frozen sections or thick sections fixed in 4% paraformaldehyde and in cultured cells. By immunoblotting this antibody detects two bands, ~180 and ~200 kDa, which merge into a single NFH line on two-dimensional gels. Antibody should be titrated for optimal results in individual systems.
          Storage +2°C to +8°C
          Avoid freeze/thaw
          Do Not Freeze Ok to freeze
          Special InstructionsFollowing initial thaw, aliquot and freeze (-20°C).
          Toxicity Standard Handling
          ReferencesTrapp, B.D., et al. 1998. N. Engl. J. Med. 338, 278.
          King, C.E., et al. 1997. Neuroreport. 8, 1663.
          Campbell, M.J., et al. 1991. Brain Res. 539, 133.
          Campbell, M.J., et al. 1989. J. Comp. Neurol. 282, 191.
          Sternberger, L.A., et al. 1983. Proc. Natl. Acad. Sci. USA 80, 6126.