TSPAN9 Polyclonal Antibody, APC-Cy5.5 Conjugated
Applications
Reactivity
Overview | |
Catalog # | bs-9448R-APC-Cy5.5 |
Product Name | TSPAN9 Polyclonal Antibody, APC-Cy5.5 Conjugated |
Applications | WB, FCM, IF(IHC-P) |
Reactivity | Human, Mouse, Rat |
Specifications | |
Conjugation | APC-Cy5.5 |
Host | Rabbit |
Source | KLH conjugated synthetic peptide derived from human TSPAN9 |
Immunogen Range | 131-239/239 |
Clonality | Polyclonal |
Isotype | IgG |
Concentration | 1ug/ul |
Purification | Purified by Protein A. |
Storage Buffer | Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
Storage Condition | Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles. |
Target | |
Gene ID | 10867 |
Swiss Prot | O75954 |
Subcellular location | Extracellular |
Synonyms | NET5; NET-5; PP1057; Tetraspanin-9; Tspan-9; Tetraspan NET-5; TSPAN9 |
Background | The tetraspanin family is a group of cell surface proteins that regulate cell development, activation, growth and motility. Each member contains four hydrophobic domains and participates in the mediation of signal transduction. NET-5, also known as TSPAN9 (tetraspanin 9), is a 239 amino acid multi-pass membrane protein that belongs to the tetraspanin (TM4SF) family. NET-5 forms a complex with GPVI in the tetraspanin microdomains on the platelet surface, and is encoded by a gene that maps to human chromosome 12p13.33. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders. |
Application Dilution | |
WB | 1:300-5000 |
FCM | 1:20-100 |
IF(IHC-P) | 1:50-200 |