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

TSPY-Like 6 antibody

TSPYL6 Reactivity: Human IHC, ELISA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7343146
  • Target See all TSPY-Like 6 (TSPYL6) products
    TSPY-Like 6 (TSPYL6)
    Reactivity
    • 26
    • 2
    • 1
    Human
    Host
    • 25
    • 1
    Rabbit
    Clonality
    • 26
    Polyclonal
    Conjugate
    • 9
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TSPY-Like 6 antibody is un-conjugated
    Application
    • 18
    • 14
    • 13
    • 13
    • 13
    • 5
    • 2
    • 1
    Immunohistochemistry (IHC), ELISA
    Cross-Reactivity
    Human
    Purification
    Antigen affinity purification
    Immunogen
    Synthetic peptide of Human TSPYL6
    Isotype
    IgG
  • Application Notes
    ELISA:1:2000-1:5000, IHC:1:25-1:100,
    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
    TSPY-Like 6 (TSPYL6)
    Alternative Name
    TSPYL6 (TSPYL6 Products)
    Synonyms
    TSPY like 6 antibody, TSPYL6 antibody
    Background

    Background: TSPYL6 (Testis-specific Y-encoded-like protein 6) is a 410 amino acid member of the nucleosome assembly protein (NAP) family. TSPYL6 is believed to be similar to Testis-specific Y-encoded protein 1 in form and function. The gene that encodes TSPYL6 is found on chromosome 2 which consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr m syndrome is due to mutations in the ALMS1 gene.

    Aliases: TSPY-like 6

    UniProt
    Q8N831
You are here: