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

Small Integral Membrane Protein 19 (SMIM19) antibody (Cy5) Primary Antibody

SMIM19 Reactivity: Human, Mouse, Rat IF (p) Host: Rabbit Polyclonal Cy5
Catalog No. ABIN1705104
$442.20
Plus shipping costs $45.00
100 μL
local_shipping Shipping to: United States
Delivery in 11 to 16 Business Days
  • Target
    Small Integral Membrane Protein 19 (SMIM19)
    Reactivity
    Human, Mouse, Rat
    Host
    Rabbit
    • 18
    Clonality
    Polyclonal
    • 18
    Conjugate
    Cy5
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Application
    Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    • 12
    • 4
    • 3
    • 3
    • 1
    • 1
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C8orf40
    Isotype
    IgG
  • Application Notes
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 1 % BSA, 50 % glycerol and 0.09 % sodium azide.
    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
    4 °C
    Storage Comment
    Store at 4°C
    Expiry Date
    12 months
  • Target
    Small Integral Membrane Protein 19 (SMIM19)
    Alternative Name
    C8orf40
    Synonyms
    C8orf40, AI316807, BG694986, EST-c39, small integral membrane protein 19, SMIM19, Smim19
    Background

    Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf40 gene product has been provisionally designated C8orf40 pending further characterization.

    Synonyms: C8orf40, CH040_HUMAN, UPF0697 protein C8orf40.

    Gene ID
    114926
You are here:
help Support