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Nhs anticorps (AA 600-900)

Nhs Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7268827
  • Antigène Voir toutes Nhs Anticorps
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Épitope
    AA 600-900
    Reactivité
    Humain
    Hôte
    • 1
    Lapin
    Clonalité
    • 1
    Polyclonal
    Conjugué
    • 1
    Cet anticorp Nhs est non-conjugé
    Application
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Fonction
    NHS Rabbit pAb
    Séquence
    MDQKDDHQSS SGNWSGSSST CPSQTSETIP PAASPPLTGS SHCDSELSLN TAPHANEDAS VFVTEQYNDH LDKVRGHRAN SFTSTVADLL DDPNNSNTSD SEWNYLHHHH DASCRQDFSP ERPKADSLGC PSFTSMATYD SFLEKSPSDK ADTSSHFSVD TEGYYTSMHF DCGLKGNKSY VCHYAALGPE NGQGVGASPG LPDCAWQDYL DHKRQGRPSI SFRKPKAKPT PPKRSSSLRK SDGNADISEK KEPKISSGQH LPHSSREMKL PLDFANTPSR MENANLPTKQ EPSWINQSEQ G
     Réactivité croisée
    Humain
    Attributs du produit
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein containing a sequence corresponding to amino acids 600-900 of human NHS (NP_938011.1).
    Isotype
    IgG
    Top Product
    Discover our top product Nhs Anticorps primaire
  • Indications d'application
    WB,1:200 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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 at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Autre désignation
    NHS (Nhs Produits)
    Synonymes
    anticorps CTRCT40, anticorps CXN, anticorps SCML1, anticorps NHS actin remodeling regulator, anticorps NHS
    Sujet
    This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.,NHS,CTRCT40,CXN,SCML1,Neuroscience,NHS
    Poids moléculaire
    160kDa/176kDa/179kDa
    ID gène
    4810
    UniProt
    Q6T4R5
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