Millipore Sigma Vibrant Logo

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

FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.
View Products on Sigmaaldrich.com
NE1023
  
Prix en cours de récupération
Le prix n'a pas pu être récupéré
La quantité minimale doit être un multiple de
Maximum Quantity is
À la validation de la commande Plus d'informations
Vous avez sauvegardé ()
 
—
Demander le prix
—
Disponibilité limitée Disponibilité limitée
En stock 
Interrompu(e)
Disponible en quantités limitées
Disponibilité à confirmer
    Pour le restant : Nous vous tiendrons informé
      Pour le restant : Nous vous tiendrons informé
      Nous vous tiendrons informé
      Contacter le Service Clients
      Contact Customer Service

       

      Contacter le Service Clients

      Aperçu

      Replacement Information

      Tableau de caractéristiques principal

      Species ReactivityHostAntibody Type
      MaMMonoclonal Antibody
      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
      Quality LevelMQ100
      Applications
      Key Applications Enzyme-Linked Immunosorbent Assay
      Frozen Sections
      Immunoblotting (Western Blotting)
      Immunocytochemistry
      Paraffin Sections
      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
      Global Trade Item Number
      Référence GTIN
      NE1023 0

      Documentation

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

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      Anti-Neurofilament H Non-Phosphorylated Mouse mAb (SMI-32) Certificats d'analyse

      TitreNuméro de lot
      NE1023

      Références bibliographiques

      Aperçu de la référence bibliographique
      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.
      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.

      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 Avoid freeze/thaw
      +2°C to +8°C
      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.