In eukaryotic cells, the Golgi apparatus receives newly synthesized proteins from the endoplasmic reticulum and delivers them after covalent modification to their destination in the cell. For membrane-directed proteins this process is believed to be carried out via vesicular transport. Correct vesicular transport is determined by specific pairing of vesicle-associated SNAREs (v-SNAREs) with those on the target membrane (t-SNAREs). This complex then recruits soluble NSF attachment proteins (SNAPs) and N-ethylmaleimide-sensitive factor (NSF) to form the highly stable SNAP receptor (SNARE) complex. The formation of a SNARE complex pulls the vesicle and target membrane together and may provide the energy to drive fusion of the lipid bilayers. A SNAP 25 related t-SNARE protein, SNAP 23, is required for exocytosis, suggesting that SNAP 23 may play an important role in membrane fusion events. The human SNAP 23 gene encodes two SNAP 23 isoforms, SNAP 23A and SNAP 23B. SNAP 23B is identical to a fragment of SNAP 23A, but SNAP 23B lacks 53 amino acid residues (90 to 142) that are present in SNAP 23A. SNAP 23 is ubiquitously expressed and is an important regulator of transport vesicle docking and fusion in all mammalian cells.
Background References
1. Kociucka B et al. Expression of genes involved in lipid droplet formation (BSCL2, SNAP23 and COPA) during porcine in vitro adipogenesis. J Appl Genet 57:505-510 (2016).
2. Williams KC & Coppolino MG. SNARE-dependent interaction of Src, EGFR and 1 integrin regulates invadopodia formation and tumor cell invasion. J Cell Sci 127:1712-25 (2014).
Sequence Similarity
Belongs to the SNAP-25 family.
Tissue Specificity
Ubiquitous. Highest levels where found in placenta.
Western blot analysis of SNAP23 on different lysates with Rabbit anti-SNAP23 antibody (ET1704-95) at 1/2,000 dilution.
Lane 1: HeLa cell lysate (20 µg/Lane) Lane 2: HepG2 cell lysate (20 µg/Lane) Lane 3: HEK-293 cell lysate (20 µg/Lane) Lane 4: PC-12 cell lysate (20 µg/Lane) Lane 5: Mouse pancreas tissue lysate (40 µg/Lane)
Predicted band size: 23 kDa Observed band size: 25 kDa
Exposure time: 3 minutes; ECL: K1802;
4-20% SDS-PAGE gel.
Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1704-95) at 1/2,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.
Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-SNAP23 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes.The tissues were blocked in 1% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1704-95, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"