NPHP1 抗体
Quick Overview for NPHP1 抗体 (ABIN7253698)
抗原
See all NPHP1 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Antigen affinity purification
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免疫原
- Fusion protein of human NPHP1
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亚型
- IgG
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anti-Nephronophthisis 1 (Juvenile) (NPHP1) (AA 345-614) antibody
NPHP1 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) (AA 1-121) antibodyNPHP1 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) (AA 1-109) antibodyNPHP1 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) antibodyNPHP1 适用: 人, 小鼠, 大鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) antibodyNPHP1 适用: 人 WB 宿主: 兔 Monoclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) antibody (FITC)NPHP1 适用: 人 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal FITC
anti-Nephronophthisis 1 (Juvenile) (NPHP1) (AA 467-516) antibodyNPHP1 适用: 人, 小鼠, 大鼠, 犬, Cow, 豚鼠, 马, Pig, 兔, Bat, 猴, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) (AA 1-109) antibodyNPHP1 适用: 人 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) (AA 1-121) antibodyNPHP1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Nephronophthisis 1 (Juvenile) (NPHP1) antibody (HRP)NPHP1 适用: 人 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal HRP
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应用备注
- WB 1:500-1:2000, IHC 1:50-1:300, ELISA 1:5000-1:10000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1.02 mg/mL
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缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- NPHP1 (Nephronophthisis 1 (Juvenile) (NPHP1))
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别名
- NPHP1
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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.
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分子量
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Observed_MW: Refer to figures
Calculated_MW: 83 kDa
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UniProt
- O15259
抗原
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