The ZNF592 Polyclonal Antibody (PACO05796) is an essential tool for researchers studying ZNF592, a zinc finger protein involved in RNA splicing regulation. This antibody, generated in rabbits, exhibits high reactivity with human samples and is validated for use in Western blotting and immunofluorescence applications. It specifically targets the ZNF592 protein, allowing for precise detection and analysis in various cell types, making it ideal for investigations in molecular biology and genetic research.ZNF592 is a key player in gene expression regulation, particularly in the processing of precursor mRNA molecules into mature mRNA.
Its role in RNA splicing makes it a crucial factor in the control of gene expression and ultimately cellular function. Research into ZNF592 is essential for gaining insights into genetic disorders, cancer development, and other diseases influenced by aberrant RNA processing.With its ability to specifically target and detect ZNF592, the PACO05796 antibody is a valuable asset for scientists seeking to explore the intricate mechanisms of RNA splicing regulation and its impacts on human health and disease.
Antibody Name:
ZNF592 Antibody (PACO05796)
Antibody SKU:
PACO05796
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, WB, IHC
Recommended Dilutions:
ELISA:1:40000, WB:1:500-1:2000, IHC:1:100-1:300
Species Reactivity:
Human, Mouse
Immunogen:
Synthesized peptide derived from the C-terminal region of human ZNF592.
Form:
Liquid
Storage Buffer:
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Purification Method:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Clonality:
Polyclonal
Isotype:
IgG
Conjugate:
Non-conjugated
Synonyms:
ZNF592; KIAA0211; Zinc finger protein 592
UniProt Protein Function:
ZNF592: a probable transcriptional regulator of the krueppel C2H2-type zinc-finger protein family.Protein type: C2H2-type zinc finger proteinChromosomal Location of Human Ortholog: 15q25.3Molecular Function: protein bindingDisease: Galloway-mowat Syndrome
