The SNX18 Antibody (CAB10337) is a high-quality antibody developed for reliable detection and analysis of target proteins. This antibody, generated in rabbits, is highly specific for human SNX18 and has been validated for use in Western blot applications.SNX18 is a member of the sorting nexin family, which are involved in endosomal sorting and membrane trafficking. Research has shown that SNX18 plays a critical role in regulating membrane curvature and vesicle formation, making it a key player in cellular processes such as receptor recycling and protein trafficking. By targeting SNX18 with this antibody, researchers can study its localization and function in various cell types, shedding light on its role in cellular physiology and disease pathogenesis.
This antibody is validated for use in WB, ELISA applications and has demonstrated reactivity against Human, Mouse, Rat samples.
Product Name:
SNX18 Antibody
SKU:
CAB10337
Size:
20μL, 100μL
Reactivity:
Human, Mouse, Rat
Conjugate:
Unconjugated
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members, but contains a SH3 domain. Multiple transcript variants encoding different isoforms have been found for this gene.
Purification Method
Affinity purification
Gene ID
112574
RRID
AB_2757882
Buffer Information
Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS containing 50% glycerol, preserved with proclin300 or sodium azide, pH 7.3.
Western blot analysis of various lysates using SNX18 Rabbit pAb (CAB10337) at 1:1000 dilution. Secondary antibody: HRP-conjugated 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 Basic Kit (AbGn00020). Exposure time: 60s.
