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VSIG1 antibody

VSIG1 Reactivity: Human ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7193032
  • Target See all VSIG1 Antibodies
    VSIG1 (V-Set and Immunoglobulin Domain Containing 1 (VSIG1))
    Reactivity
    • 28
    • 8
    • 5
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 27
    • 9
    • 2
    • 1
    Rabbit
    Clonality
    • 31
    • 8
    Polyclonal
    Conjugate
    • 15
    • 6
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This VSIG1 antibody is un-conjugated
    Application
    • 24
    • 13
    • 13
    • 8
    • 8
    • 4
    • 4
    • 1
    ELISA, Immunohistochemistry (IHC)
    Cross-Reactivity
    Human
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of Human VSIG10
    Isotype
    IgG
  • Application Notes
    ELISA:1:2000-1:10000, IHC:1:30-1:150,
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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,-80 °C
    Storage Comment
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Target
    VSIG1 (V-Set and Immunoglobulin Domain Containing 1 (VSIG1))
    Alternative Name
    VSIG1 (VSIG1 Products)
    Synonyms
    VSIG1 antibody, vsig1 antibody, CHT1 antibody, 1700062D20Rik antibody, GPA34 antibody, dJ889N15.1 antibody, 4930405J24Rik antibody, ctx antibody, ctx-A antibody, gpa34 antibody, V-set and immunoglobulin domain containing 1 antibody, V-set and immunoglobulin domain containing 1 L homeolog antibody, VSIG1 antibody, vsig1 antibody, Vsig1 antibody, vsig1.L antibody
    Background

    Background: It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fc receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene BCL3. The LOC147645 gene product has been provisionally designated LOC147645 pending further characterization.

    Aliases: V-set and immunoglobulin domain containing 10

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