The ZNF273 Polyclonal Antibody (CAB14847) is a valuable tool for researchers studying the ZNF273 protein, a transcription factor implicated in gene regulation and DNA binding. This antibody, produced in rabbits, exhibits high reactivity with human samples and has been validated for use in immunofluorescence and immunohistochemistry applications. By binding to the ZNF273 protein, the antibody allows for the detection and analysis of this important molecule in various cell types, making it an ideal choice for studies in molecular biology and genetics.
ZNF273 is known to play a crucial role in controlling gene expression and cell differentiation, making it a key player in various biological processes. Understanding the function of ZNF273 is essential for unraveling its role in development, disease, and cellular homeostasis. Research involving ZNF273 could lead to insights into genetic disorders, cancer progression, and stem cell biology, making this antibody a valuable asset for investigators exploring these areas of study.
Product Name:
ZNF273 Rabbit Polyclonal Antibody
SKU:
CAB14847
Size:
20uL, 100uL
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human
Immunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 210-260 of human ZNF273 (NP_066971.2).
This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with 13 C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in transcriptional regulation. Alternative splicing results in multiple transcript variants.
Purification Method:
Affinity purification
Gene ID:
10793
Storage Buffer:
Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.01% thimerosal,50% glycerol,pH7.3.
Western blot analysis of various lysates, using ZNF273 antibody (CAB14847) at 1:400 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution.Lysates/proteins: 25μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Enhanced Kit (AbGn00021).Exposure time: 60s.
