The ZNF287 Polyclonal Antibody (PACO03038) is a valuable tool for researchers studying ZNF287, a transcription factor involved in gene regulation and cell differentiation. This antibody, generated in rabbits, exhibits high specificity and sensitivity towards human samples, making it suitable for use in a variety of research applications, including Western blotting.ZNF287 plays a crucial role in controlling gene expression and cell fate determination, making it a key player in developmental processes and disease pathways. By targeting the ZNF287 protein, this antibody enables precise detection and analysis of its function in various cell types, offering valuable insights for studies in molecular biology and biomedical research.
The ZNF287 Polyclonal Antibody is essential for investigating the role of ZNF287 in various cellular processes and disease mechanisms, providing researchers with a powerful tool for advancing their understanding of gene regulation and potential therapeutic targets. Its reliability and performance make it a valuable asset for any laboratory conducting research in the fields of genetics, cell biology, and disease pathology.
Antibody Name:
ZNF287 Antibody
Antibody SKU:
PACO03038
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, WB, IHC
Recommended Dilutions:
WB:1:500-1:2000, IHC:1:100-1:300
Species Reactivity:
Human
Immunogen:
synthesized peptide derived from the Internal region of human ZNF287.
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:
ZNF287; ZKSCAN13; Zinc finger protein 287; Zinc finger protein with KRAB and SCAN domains 13
UniProt Protein Function:
May be involved in transcriptional regulation.
UniProt Protein Details:
NCBI Summary:
This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]
