Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.05% proclin300,50% glycerol,pH7.3.
规格:
50 μL/100 μL/200 μL
规格:
50 μL
产品价格:
¥900.0
规格:
100 μL
产品价格:
¥1500.0
规格:
200 μL
产品价格:
¥2450.0
产品名称:NPHP1 Rabbit pAb 货号:A6674 背景:This gene encodes a protein with src homology domain 3 (SH3) patterns. This protein interacts with Crk-associated substrate, and it appears to function in the control of cell division, as well as in cell-cell and cell-matrix adhesion signaling, likely as part of a multifunctional complex localized in actin- and microtubule-based structures. Mutations in this gene cause familial juvenile nephronophthisis type 1, a kidney disorder involving both tubules and glomeruli. Defects in this gene are also associated with Senior-Loken syndrome type 1, also referred to as juvenile nephronophthisis with Leber amaurosis, which is characterized by kidney and eye disease, and with Joubert syndrome type 4, which is characterized by cerebellar ataxia, oculomotor apraxia, psychomotor delay and neonatal breathing abnormalities, sometimes including retinal dystrophy and renal disease. Multiple transcript variants encoding different isoforms have been found for this gene. 别名:NPH1; JBTS4; SLSN1; NPHP1 宿主:Rabbit 反应物种:Human, Mouse, Rat 验证应用:ELISA,WB,IHC-P,IF/ICC 免疫原:Recombinant fusion protein containing a sequence corresponding to amino acids 463-732 of human NPHP1 (NP_997064.2). 基因ID:4867 存储缓冲液:Store at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.05% proclin300,50% glycerol,pH7.3.