WB result of PRSS35 Recombinant Rabbit mAb
Primary antibody: PRSS35 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: PC-3 whole cell lysate 20 µg
Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 47 kDa
Observed MW: 60 kDa
Product Details
Product Details
Product Specification
| Host | Rabbit |
| Antigen | PRSS35 |
| Synonyms | Inactive serine protease 35; C6orf158 |
| Immunogen | Synthetic Peptide |
| Location | Secreted |
| Accession | Q8N3Z0 |
| Clone Number | S-3769-241 |
| Antibody Type | Recombinant mAb |
| Isotype | IgG |
| Application | WB, IHC-P, ICC |
| Reactivity | Hu, Ms, Rt |
| Positive Sample | PC-3, mouse liver, rat liver |
| Purification | Protein A |
| Concentration | 0.5 mg/ml |
| Conjugation | Unconjugated |
| Physical Appearance | Liquid |
| Storage Buffer | PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300 |
| Stability & Storage | 12 months from date of receipt / reconstitution, -20 °C as supplied |
Dilution
| application | dilution | species |
| WB | 1:1000-1:2000 | Hu, Ms, Rt |
| IHC-P | 1:1000 | Hu, Ms, Rt |
| ICC | 1:500 | Hu |
Background
PRSS35, also known as serine protease 35 or neurosin, is a member of the S1 family of chymotrypsin-like serine proteases that is predominantly expressed in the central nervous system, particularly within neurons and oligodendrocytes. This enzyme plays a critical role in various physiological processes, including the regulation of myelin maintenance, synaptic plasticity, and the processing of extracellular matrix proteins such as myelin basic protein (MBP) and proteolipid protein (PLP). Research suggests that PRSS35 is involved in the turnover of myelin components, thereby influencing nerve conduction velocity and overall neural integrity, while its dysregulation or overexpression has been implicated in pathological conditions such multiple sclerosis, Alzheimer’s disease, and certain types of cancer, where it may contribute to tissue remodeling, inflammation, and tumor progression through the degradation of specific substrates and modulation of cell signaling pathways.
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Western Blot
WB result of PRSS35 Recombinant Rabbit mAb
Primary antibody: PRSS35 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: mouse liver lysate 20 µg
Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 47 kDa
Observed MW: 60 kDa
WB result of Recombinant Rabbit mAb
Primary antibody: PRSS35 Recombinant Rabbit mAb at 1/1000 dilution
Lane 1: rat liver lysate 20 µg
Secondary antibody: Goat Anti- rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
Predicted MW: 47 kDa
Observed MW: 60 kDa
Immunohistochemistry
IHC shows positive staining in paraffin-embedded human liver. Anti-PRSS35 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded human liver cancer. Anti-PRSS35 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded mouse kidney. Anti-PRSS35 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
IHC shows positive staining in paraffin-embedded rat liver. Anti-PRSS35 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
Immunocytochemistry
ICC shows positive staining in PC-3 cells. Anti-PRSS35 antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 100% ice-cold methanol and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).
