The SNX33 Polyclonal Antibody (PAC020576) is a valuable tool for researchers studying SNX33, a protein involved in endosomal sorting and trafficking. This antibody, produced in rabbits, is highly specific to human samples and has been validated for use in Western blot applications. By detecting and binding to the SNX33 protein, this antibody enables the analysis of its expression and function in various cellular processes.SNX33 is known for its role in endosomal sorting and membrane trafficking, making it essential for maintaining cellular homeostasis and regulating signaling pathways.
Research on SNX33 is important for understanding its contribution to cellular processes such as receptor internalization, lysosomal targeting, and vesicle formation. This antibody provides researchers with a reliable tool to investigate the function of SNX33 in various cellular contexts, including studies on intracellular trafficking, signaling transduction, and membrane dynamics.
Antibody Name:
SNX33 Antibody (PACO20576)
Antibody SKU:
PACO20576
Size:
50ul
Host Species:
Rabbit
Tested Applications:
ELISA, IHC
Recommended Dilutions:
ELISA:1:1000-1:2000, IHC:1:10-1:50
Species Reactivity:
Human, Mouse
Immunogen:
Synthetic peptide of human SNX33
Form:
Liquid
Storage Buffer:
-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Purification Method:
Antigen affinity purification
Clonality:
Polyclonal
Isotype:
IgG
Conjugate:
Non-conjugated
The image on the left is immunohistochemistry of paraffin-embedded Human liver cancer tissue using PACO20576(SNX33 Antibody) at dilution 1/20, on the right is treated with synthetic peptide. (Original magnification: x200).
Background:
SNX33 (sorting nexin-33), also known as SH3PX3, SH3PXD3C or SNX30, is a 574 amino acid, protein that interacts with ADAM15 and FAS-L. Belonging to the sorting nexin family, SNX33 contains one BAR domain, one PX (phox homology) domain and one SH3 domain. The gene that encodes SNX33 consists of over 14,000 bases and maps to human chromosome 15q24.2. Housing approximately 106 million base pairs and encoding more than 700 genes, chromosome 15 makes up about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region.
Synonyms:
sorting nexin 33
UniProt Protein Function:
SNX33: Belongs to the sorting nexin family.Protein type: Unknown functionChromosomal Location of Human Ortholog: 15q24.2Cellular Component: cytoplasmic membrane-bound vesicle; cytosol; endosome; extrinsic to membrane; membraneMolecular Function: identical protein binding; phosphoinositide binding; protein bindingBiological Process: cytokinesis after mitosis; endocytosis; endosome organization and biogenesis; endosome transport; negative regulation of endocytosis; positive regulation of membrane protein ectodomain proteolysis; protein import; vesicle organization and biogenesis
UniProt Protein Details:
NCBI Summary:
The protein encoded by this gene is involved in cytoskeletal reorganization, vesicle trafficking, endocytosis, and mitosis. The encoded protein is essential for the creation of the cleavage furrow during mitosis and for completion of mitosis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]