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Nhs antibody (AA 600-900)

Nhs Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7268827
  • Target See all Nhs Antibodies
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Binding Specificity
    AA 600-900
    Reactivity
    Human
    Host
    • 1
    Rabbit
    Clonality
    • 1
    Polyclonal
    Conjugate
    • 1
    This Nhs antibody is un-conjugated
    Application
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    NHS Rabbit pAb
    Sequence
    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
    Cross-Reactivity
    Human
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    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 Primary Antibody
  • Application Notes
    WB,1:200 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Nhs (Nance-Horan Syndrome (Congenital Cataracts and Dental Anomalies) (Nhs))
    Alternative Name
    NHS (Nhs Products)
    Synonyms
    CTRCT40 antibody, CXN antibody, SCML1 antibody, NHS actin remodeling regulator antibody, NHS antibody
    Background
    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
    Molecular Weight
    160kDa/176kDa/179kDa
    Gene ID
    4810
    UniProt
    Q6T4R5
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