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SNRPN anticorps (AA 14-174)

Cet anticorps Souris Monoclonal détecte spécifiquement SNRPN dans WB, IF, BI et IHC (f). Il présente une réactivité envers Humain, Souris, Rat et Chien et a été mentionné dans 6+ publications.
N° du produit ABIN968086

Aperçu rapide pour SNRPN anticorps (AA 14-174) (ABIN968086)

Antigène

Voir toutes SNRPN Anticorps
SNRPN (Small Nuclear Ribonucleoprotein Polypeptide N (SNRPN))

Reactivité

  • 24
  • 9
  • 8
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat, Chien

Hôte

  • 21
  • 4
Souris

Clonalité

  • 23
  • 2
Monoclonal

Conjugué

  • 20
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp SNRPN est non-conjugé

Application

  • 24
  • 12
  • 11
  • 5
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), BioImaging (BI), Immunohistochemistry (Formalin-fixed Sections) (IHC (f))

Clone

8-SMN
  • Épitope

    • 6
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 14-174

     Réactivité croisée

    Souris, Rat (Rattus), Chien

    Attributs du produit

    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. Please refer to us for technical protocols.
    3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
    4. Source of all serum proteins is from USDA inspected abattoirs located in the United States.

    Purification

    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

    Immunogène

    Human SMN aa. 14-174

    Isotype

    IgG1
  • Commentaires

    Related Products: ABIN968587, ABIN967389

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    250 μg/mL

    Buffer

    Aqueous buffered solution containing BSA, glycerol, and ≤0.09 % sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store undiluted at -20°C.
  • Briese, Richter, Sattelle, Ulfig: "SMN, the product of the spinal muscular atrophy-determining gene, is expressed widely but selectively in the developing human forebrain." dans: The Journal of comparative neurology, Vol. 497, Issue 5, pp. 808-16, (2006) (PubMed).

    Côté, Boisvert, Boulanger, Bedford, Richard: "Sam68 RNA binding protein is an in vivo substrate for protein arginine N-methyltransferase 1." dans: Molecular biology of the cell, Vol. 14, Issue 1, pp. 274-87, (2003) (PubMed).

    Claus, Doring, Gringel, Muller-Ostermeyer, Fuhlrott, Kraft, Grothe: "Differential intranuclear localization of fibroblast growth factor-2 isoforms and specific interaction with the survival of motoneuron protein." dans: The Journal of biological chemistry, Vol. 278, Issue 1, pp. 479-85, (2002) (PubMed).

    Wang, Reddy, Shen: "Higher order arrangement of the eukaryotic nuclear bodies." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 99, Issue 21, pp. 13583-8, (2002) (PubMed).

    Cifuentes-Diaz, Frugier, Tiziano, Lacène, Roblot, Joshi, Moreau, Melki: "Deletion of murine SMN exon 7 directed to skeletal muscle leads to severe muscular dystrophy." dans: The Journal of cell biology, Vol. 152, Issue 5, pp. 1107-14, (2001) (PubMed).

    Lefebvre, Bürglen, Reboullet, Clermont, Burlet, Viollet, Benichou, Cruaud, Millasseau, Zeviani: "Identification and characterization of a spinal muscular atrophy-determining gene." dans: Cell, Vol. 80, Issue 1, pp. 155-65, (1995) (PubMed).

  • Antigène

    SNRPN (Small Nuclear Ribonucleoprotein Polypeptide N (SNRPN))

    Autre désignation

    SMN

    Sujet

    SMN (survival motor neuron) was discovered as a candidate gene, located in chromosome 5q13, for the fatal autosomal Spinal muscular atrophy (SMA) disorder. The SMN gene was missing or interrupted in a significant number of patients with SMA. The SMN protein is 294 amino acids and migrates with apparent molecular weight of 40 kDa. In addition to the cytoplasm, other studies localized SMN in dots of 0.1-1.0 µm within the nucleus. These novel nuclear structures were named gems and found associated to coiled bodies. It was also found that SMN interacts with the RGG box of hnRNP U and fibrillarin. Therefore, the biochemical function of SMN may be in the regulation of mRNA metabolism.
    Synonyms: Survival Motor Neuron

    Poids moléculaire

    40 kDa
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