The ZNF287 Polyclonal Antibody (PACO23284) is a valuable tool for researchers studying the zinc finger protein ZNF287. This antibody, raised in rabbits, exhibits high reactivity with human samples and is validated for use in various applications, including Western blotting. By specifically binding to the ZNF287 protein, this antibody enables the detection and analysis of ZNF287 in a variety of cell types.ZNF287 is a transcription factor that plays a critical role in gene regulation and cell differentiation. Its involvement in various cellular processes makes it a key target for research in fields such as developmental biology, cancer biology, and stem cell research.
Understanding the function and regulation of ZNF287 can provide insights into the mechanisms underlying diseases and potential therapeutic targets.Overall, the ZNF287 Polyclonal Antibody (PACO23284) is a valuable tool for researchers investigating the role of ZNF287 in a wide range of biological processes and diseases. Its high specificity and reactivity make it a reliable choice for studies aimed at elucidating the functions of this important protein.
Synthesized peptide derived from internal of human ZNF287.
Form:
Liquid
Storage Buffer:
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Purification Method:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Clonality:
Polyclonal
Isotype:
IgG
Conjugate:
Non-conjugated
Western blot analysis of extracts from NIH-3T3 cells, using ZNF287 antibody.
Immunohistochemistry analysis of paraffin-embedded human brain tissue using ZNF287 antibody.
Background:
May be involved in transcriptional regulation.
Synonyms:
Zinc finger protein with KRAB and SCAN domains 13; Zinc finger protein 287; ZNF287; ZKSCAN13;
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]
