Anticorps Recombinant de lapin anti-FAM38B
FAM38B Recombinant Antibody for WB, Cytometric bead array, Indirect ELISA
Hôte / Isotype
Lapin / IgG
Réactivité testée
Humain
Applications
WB, Cytometric bead array, Indirect ELISA
Conjugaison
Non conjugué
CloneNo.
240406E5
N° de cat : 83488-4-PBS
Synonymes
Galerie de données de validation
Informations sur le produit
83488-4-PBS cible FAM38B dans les applications de WB, Cytometric bead array, Indirect ELISA et montre une réactivité avec des échantillons Humain
| Réactivité | Humain |
| Hôte / Isotype | Lapin / IgG |
| Clonalité | Recombinant |
| Type | Anticorps |
| Immunogène | FAM38B Protéine recombinante Ag24528 |
| Nom complet | family with sequence similarity 38, member B |
| Masse moléculaire calculée | 318 kDa |
| Poids moléculaire observé | 250-310 kDa, 80 kDa |
| Numéro d’acquisition GenBank | AB527139 |
| Symbole du gène | FAM38B |
| Identification du gène (NCBI) | 63895 |
| Conjugaison | Non conjugué |
| Forme | Liquide |
| Méthode de purification | Purification par protéine A |
| Tampon de stockage | PBS only |
| Conditions de stockage | Store at -80°C. 20ul contiennent 0,1% de BSA. |
Informations générales
FAM38B, also named as PIEZO2, is a mechanosensitive, rapidly inactivating (RI) ion channel which is open and converts the mechanical stimulus signals into bioelectrical signals after stimulated by mechanical signals. FAM38B has been recently identified in dorsal root ganglion (DRG) neurons to mediate tactile transduction. It plays an important role in the biological process, maintaining cell metabolism and cell migration. Loss-of-function mutations in the human FAM38B gene cause an autosomal recessive syndrome of muscular atrophy with perinatal respiratory distress, arthrogryposis, and scoliosis.The 80 kDa band detected by SDS-PAGE can be caused by alternative splicing (PMID: 34335288, 37227654).









