The TSPYL6 Polyclonal Antibody (PAC020779) is a valuable tool for researchers studying TSPYL6, a protein that plays a role in various cellular processes, including gene regulation and cell proliferation. This antibody, produced in rabbits, is highly specific to human samples and is validated for use in a range of applications, including Western blotting.TSPYL6 has been implicated in cancer development and progression, making it an important target for cancer research.
By using this antibody, researchers can effectively detect and analyze TSPYL6 expression in different cell types, providing insight into its function and potential therapeutic applications.With its high reactivity and specificity, the TSPYL6 Polyclonal Antibody is a reliable tool for investigating the role of TSPYL6 in cancer and other diseases, ultimately contributing to the development of targeted therapies and personalized medicine.
Antibody Name:
TSPYL6 Antibody (PACO20779)
Antibody SKU:
PACO20779
Size:
50ul
Host Species:
Rabbit
Tested Applications:
ELISA, IHC
Recommended Dilutions:
ELISA:1:2000-1:5000, IHC:1:25-1:100
Species Reactivity:
Human
Immunogen:
Synthetic peptide of human TSPYL6
Form:
Liquid
Storage Buffer:
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Purification Method:
Antigen affinity purification
Clonality:
Polyclonal
Isotype:
IgG
Conjugate:
Non-conjugated
The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using PACO20779(TSPYL6 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200).
The image on the left is immunohistochemistry of paraffin-embedded Human ovarian cancer tissue using PACO20779(TSPYL6 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200).
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.
Synonyms:
TSPY-like 6
UniProt Protein Function:
TSPYL6: Belongs to the nucleosome assembly protein (NAP) family.Protein type: Unknown functionChromosomal Location of Human Ortholog: 2p16.2
