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Nhs Antikörper (AA 600-900)

Nhs Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7268827
  • Target Alle Nhs Antikörper anzeigen
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Bindungsspezifität
    AA 600-900
    Reaktivität
    Human
    Wirt
    • 1
    Kaninchen
    Klonalität
    • 1
    Polyklonal
    Konjugat
    • 1
    Dieser Nhs Antikörper ist unkonjugiert
    Applikation
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Verwendungszweck
    NHS Rabbit pAb
    Sequenz
    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
    Kreuzreaktivität
    Human
    Produktmerkmale
    Polyclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 600-900 of human NHS (NP_938011.1).
    Isotyp
    IgG
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  • Applikationshinweise
    WB,1:200 - 1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Andere Bezeichnung
    NHS (Nhs Produkte)
    Synonyme
    CTRCT40 antikoerper, CXN antikoerper, SCML1 antikoerper, NHS actin remodeling regulator antikoerper, NHS antikoerper
    Hintergrund
    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
    Molekulargewicht
    160kDa/176kDa/179kDa
    Gen-ID
    4810
    UniProt
    Q6T4R5
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