The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use a concentration of 1 µg/ml. Predicted molecular weight: 65 kDa. Good results were obtained when blocked with 5% non-fat dry milk in 0.05% PBS-T.
組織特異性Isoform 1 and isoform 3 are widely expressed with highest levels in retina and testis, with isoform 1 being the mot abundant in all tissues tested.
関連疾患Defects in FAM161A are the cause of retinitis pigmentosa type 28 (RP28) [MIM:606068]. A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
Family with sequence similarity 161, member A antibody
Hypothetical protein LOC84140 antibody
Protein FAM161A antibody
Anti-FAM161A antibody 画像
Western blot - Anti-FAM161A antibody (ab115810)
Anti-FAM161A antibody (ab115810) at 1 µg/ml + Jurkat cell lysate at 10 µg
Predicted band size : 65 kDa
Anti-FAM161A antibody (ab115810) 使用論文
This product has been referenced in:
Karlstetter M et al. Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structure and leads to progressive retinal degeneration. Hum Mol GenetN/A:N/A (2014).
Read more (PubMed: 24833722) »