Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Sclerostin antibody

SOST Reactivity: Human IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7264263
  • Target See all Sclerostin (SOST) Antibodies
    Sclerostin (SOST)
    Reactivity
    • 64
    • 52
    • 35
    • 16
    • 15
    • 15
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 66
    • 3
    • 2
    • 1
    Rabbit
    Clonality
    • 67
    • 5
    Polyclonal
    Conjugate
    • 29
    • 6
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    This Sclerostin antibody is un-conjugated
    Application
    • 70
    • 30
    • 24
    • 22
    • 13
    • 12
    • 5
    • 4
    • 3
    • 2
    • 2
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human SOST (NP_079513.1).
    Isotype
    IgG
    Top Product
    Discover our top product SOST Primary Antibody
  • Application Notes
    IHC 1:50-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    Sclerostin (SOST)
    Alternative Name
    SOST (SOST Products)
    Synonyms
    LOC100313724 antibody, CDD antibody, VBCH antibody, 5430411E23Rik antibody, sclerostin antibody, LOC100313724 antibody, SOST antibody, Sost antibody
    Background
    Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease.
    Gene ID
    50964
    UniProt
    Q9BQB4
You are here:
Support