The PLCXD1 Polyclonal Antibody (PACO4695) is a valuable tool for researchers studying PLCXD1, a phosphoinositide-specific phospholipase C-like protein involved in intracellular signaling pathways. Raised in rabbits, this antibody is highly specific to human samples and is validated for use in Western blot applications. It enables the detection and analysis of PLCXD1 protein in various cell types, making it ideal for studies in cell biology and signal transduction research.PLCXD1 plays a key role in regulating cellular processes such as cell growth, differentiation, and apoptosis by modulating intracellular calcium levels and lipid signaling pathways.
Dysfunction of PLCXD1 has been implicated in various diseases, including cancer, neurodegenerative disorders, and cardiovascular diseases. Understanding the function of PLCXD1 is essential for unraveling its role in these pathologies and developing novel therapeutic strategies targeting this protein.In summary, the PLCXD1 Polyclonal Antibody is a reliable tool for researchers investigating the function of PLCXD1 in cellular processes and disease pathogenesis. Its high specificity and sensitivity make it a valuable asset in advancing our understanding of intracellular signaling mechanisms and potential therapeutic targets.
Antibody Name:
PLCXD1 Antibody
Antibody SKU:
PACO04695
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, IHC
Recommended Dilutions:
IHC:1:100-1:300
Species Reactivity:
Human
Immunogen:
synthesized peptide derived from the Internal region of human PLC-XD1.
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:
PLCXD1; PI-PLC X domain-containing protein 1
UniProt Protein Function:
PLCXD1: Chromosomal Location of Human Ortholog: Xp22.33; Yp11.32
UniProt Protein Details:
NCBI Summary:
This gene is the most terminal protein-coding gene in the pseudoautosomal (PAR) region on chromosomes X and Y. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
