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AQP4 Recombinant Rabbit mAb (S-1609-62)

AQP4,Aquaporin-4,AQP-4,Mercurial-insensitive water channel,MIWC,WCH4,Mercurial-insensitive water channel (MIWC)

货号: S0B1048

Datasheet COA
  • 价格: ¥600
  • 规格:
  • 数量:
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产品介绍 评论(0)

产品规格
  • 别名

    AQP4,Aquaporin-4,AQP-4,Mercurial-insensitive water channel,MIWC,WCH4,Mercurial-insensitive water channel (MIWC)
  • 宿主来源

    Rabbit
  • 抗原名称

    AQP4
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Cell membrane
  • Accession

    P55087
  • 克隆号

    S-1609-62
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    IHC-P, WB, IF
  • 反应种属 ?

    Hu, Ms, Rt
  • 阳性样本

    Mouse brain, rat brain, mouse kidney, rat kidney
  • 纯化方式

    Protein A
  • 浓度

    0.5 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

    PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300
  • 储存条件

    12 months from date of receipt / reconstitution, -20°C as supplied

稀释度
应用 稀释度 推荐种属
WB 1:1000 Ms, Rt
IHC-P 1:2000 Hu, Ms, Rt
IF 1:2000 Ms, Rt
背景介绍
  • Aquaporin-4 (AQP4) is a water-selective transporter that is predominantly expressed in the central nervous system (CNS), with additional expression in the kidney, lung, stomach, and skeletal muscle. Within the CNS, AQP4 is found in astrocytes and is particularly concentrated at the pial and ependymal surfaces in contact with cerebrospinal fluid (CSF) in the subarachnoid space and ventricles. AQP4 plays a critical role in maintaining water balance in the brain and spinal cord, facilitating the movement of water across cell membranes. AQP4-null mice exhibit phenotypes that suggest the involvement of AQP4 in astrocyte migration, neural signal transduction, and neuroinflammation. These mice show reduced brain swelling in cytotoxic cerebral edema but increased swelling in vasogenic edema and hydrocephalus. AQP4 deficiency also leads to increased seizure duration, impaired glial scarring, and reduced severity of autoimmune neuroinflammation. AQP4 is also implicated in the pathogenesis of neuromyelitis optica (NMO), a neuroinflammatory demyelinating disease. In NMO, autoantibodies (NMO-IgG) target AQP4, leading to astrocyte damage and inflammation. Mice administered NMO-IgG and human complement by intracerebral injection develop characteristic NMO lesions with neuroinflammation, demyelination, perivascular complement deposition, and loss of glial fibrillary acidic protein and AQP4 immunoreactivity.

  • 免疫印迹

    • WB result of AQP4 Recombinant Rabbit mAb
      Primary antibody: AQP4 Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: unboiled mouse liver lysate 20 µg
      Lane 2: unboiled mouse brain lysate 20 µg
      Negative control: unboiled mouse liver lysate
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 35 kDa
      Observed MW: 28 kDa

    • WB result of AQP4 Recombinant Rabbit mAb
      Primary antibody: AQP4 Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: unboiled rat liver lysate 20 µg
      Lane 2: unboiled rat brain lysate 20 µg
      Negative control: unboiled rat liver lysate
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 35 kDa
      Observed MW: 28 kDa

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human cerebral cortex. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human kidney. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human lung. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human skeletal muscle. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human stomach. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • Negative control: IHC shows negative staining in paraffin-embedded human liver. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded human lung squamous cell carcinoma. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded mouse cerebral cortex. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded mouse stomach. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat cerebral cortex. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

    • IHC shows positive staining in paraffin-embedded rat kidney. Anti-AQP4 antibody was used at 1/2000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

  • 免疫荧光

    • IF shows positive staining in paraffin-embedded mouse cerebral cortex. Anti- AQP4 antibody was used at 1/2000 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded mouse kidney. Anti- AQP4 antibody was used at 1/2000 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded rat cerebral cortex. Anti- AQP4 antibody was used at 1/2000 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

  • 组织表达图谱

    • Expression of AQP4 in tumor tissue

    • Expression of AQP4 in human tissue

    • Expression of AQP4 in mouse & rat tissue

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