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NPHP1 抗体 (AA 510-590)

This 兔 多克隆 antibody specifically detects NPHP1 in WB 和 ELISA. It exhibits reactivity toward 人 和 小鼠.
产品编号 ABIN8123264
发货至: 中国
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Quick Overview for NPHP1 抗体 (AA 510-590) (ABIN8123264)

抗原

See all NPHP1 抗体
NPHP1 (Nephronophthisis 1 (Juvenile) (NPHP1))

适用

  • 30
  • 15
  • 12
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 小鼠

宿主

  • 29
  • 1
兔

克隆类型

  • 29
  • 1
多克隆

标记

  • 16
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NPHP1 antibody is un-conjugated

应用范围

  • 19
  • 12
  • 8
  • 5
  • 4
  • 1
Western Blotting (WB), ELISA
  • 抗原表位

    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 510-590

    原理

    NPHP1 Antibody

    特异性

    NPHP1 Polyclonal Antibody detects endogenous levels of protein.

    纯化方法

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

    免疫原

    Synthesized peptide derived from human protein . at AA range: 510-590

    亚型

    IgG
  • 应用备注

    WB 1:500-2000 ELISA 1:5000-20000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Liquid in PBS containing 50 % glycerol, and 0.02 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C/1 year

    有效期

    12 months
  • 抗原

    NPHP1 (Nephronophthisis 1 (Juvenile) (NPHP1))

    别名

    NPHP1

    背景

    Background: 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 diffe

    Gene Name: NPHP1 NPH1

    Protein Name: Nephrocystin-1 (Juvenile nephronophthisis 1 protein)

    基因ID

    4867

    UniProt

    O15259
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