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NPHS2/Podocin antibody

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  • ¥780 - 2200
  • 康朗生物
  • kl-6597R
  • 中国/美国/德国
  • 2026年03月04日
  • WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:100-500
  • Rabbit
  • Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 供应商

      上海康朗生物科技有限公司

    • 库存

      大量

    • 目录编号

      kl-6597R

    • 克隆性

      多克隆

    • 抗原来源

      Rabbit

    • 保质期

      12个月

    • 抗体英文名

      NPHS2/Podocin antibody

    • 抗体名

      肾小球裂孔膜蛋白PDCN抗体

    • 宿主

      Rabbit

    • 适应物种

      Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,

    • 免疫原

      KLH conjugated synthetic peptide derived from human NPHS2/Podocin:231-330/383 <Extracellular>

    • 亚型

      IgG

    • 形态

      冻干粉或液体

    • 应用范围

      WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:100-500

    • 浓度

      1mg/ml

    • 保存条件

      -20 °C

    • 规格

      50ul 100ul 200ul

    NPHS2/Podocin antibody
    中文名称 肾小球裂孔膜蛋白PDCN抗体
    别    名 nephrosis 2, idiopathic, steroid resistant; NPHS2 gene; PDCN; Podocin; SRN1; PODO_HUMAN.  
    产品细节图片1
    Specific References  (2)     |     bs-6597R has been referenced in 2 publications.
    [IF=4.72] Zhang, Xiao-Liang, et al. "Vitamin D Prevents Podocyte Injury Via Regulation Of Macrophage M1/M2 Phenotype In Diabetic Nephropathy Rats." Endocrinology (2014).  WB ;  Rat.  
    PubMed:25188527
    [IF=0.00] Garovic, Vesna D., and Muthuvel Jayachandran. "DETECTING PODOCYTE INJURY IN DIABETIC NEPHROPATHY AND GLOMERULONEPHRITIS." U.S. Patent No. 20,170,003,299. 5 Jan. 2017.  Human.  
    PubMed:0
     
    规格价格 50ul/780元 购买    100ul/1380元 购买    200ul/2200元 购买    大包装/询价
    说 明 书 50ul  100ul  200ul
    研究领域 细胞生物  信号转导  细胞类型标志物  
    抗体来源 Rabbit
    克隆类型 Polyclonal
    交叉反应 Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, 
    产品应用 WB=1:500-2000 ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 IF=1:100-500 (石蜡切片需做抗原修复) 
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    分 子 量 42kDa
    细胞定位 细胞膜 
    性    状 Lyophilized or Liquid
    浓    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human NPHS2/Podocin:231-330/383 <Extracellular>
    亚    型 IgG
    纯化方法 affinity purified by Protein A
    储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
    保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
    PubMed PubMed
    产品介绍 background:
    Podocin is an important member of a group of proteins shown to be associated with the slit diaphragm. Podocin belongs to the band 7 stomatin family of lipid raft-associated proteins. It is a hairpin like integral membrane protein with intracellular N and C termini. Podocin is located at the insertion site of the slit membrane, and is thought to act as a scaffold protein required to maintain or regulate the structural integrity of the slit diaphragm. It plays a role in the regulation of glomerular permeability, acting probably as a linker between the plasma membrane and the cytoskeleton.

    Subunit:
    Interacts with nephrin/NPHS1 and KIRREL. Interacts directly with CD2AP. Interacts with DDN (By similarity).

    Subcellular Location:
    Cell membrane; Peripheral membrane protein.

    Tissue Specificity:
    Almost exclusively expressed in the podocytes of fetal and mature kidney glomeruli.

    DISEASE:
    Defects in NPHS2 are the cause of nephrotic syndrome type 2 (NPHS2) [MIM:600995]. It is a renal disorder characterized clinically by childhood onset of proteinuria, hypoalbuminemia, hyperlipidemia, and edema. Kidney biopsies show non-specific histologic changes such as focal segmental glomerulosclerosis and diffuse mesangial proliferation. The disorder is resistant to steroid treatment and progresses to end-stage renal failure in the first or second decades. Some patients show later onset of the disorder.

    Similarity:
    Belongs to the band 7/mec-2 family.

    SWISS:
    Q9NP85

    Gene ID:
    7827

    Database links:
    Entrez Gene: 7827 Human
    Entrez Gene: 170484 Mouse
    Entrez Gene: 170672 Rat
    Omim: 604766 Human
    SwissProt: Q9NP85 Human
    SwissProt: Q91X05 Mouse
    SwissProt: Q8K4G9 Rat
    Unigene: 412710 Human
    Unigene: 289099 Mouse
    Unigene: 86433 Rat



    Important Note:
    This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. 

     
    产品图片
    产品细节图片2
    Sample: Kidney (Mouse) Lysate at 40 ug
    Primary: Anti-NPHS2 (bs-6597R) at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 42 kD
    Observed band size: 47 kD
    产品细节图片3
    Paraformaldehyde-fixed, paraffin embedded (human colon cancer); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (NPHS2) Polyclonal Antibody, Unconjugated (bs-6597R) at 1:500 overnight at 4°C, followed by a conjugated secondary (sp-0023) for 20 minutes and DAB staining.
    产品细节图片4
    Blank control(blue): 293T(fixed with 2% paraformaldehyde (10 min) and then permeabilized with ice-cold 90% methanol for 30 min on ice). 
    Primary Antibody: Rabbit Anti-NPHS2/FITC Conjugated antibody (bs-6597R /FITC), Dilution: 5μg in 100 μL 1X PBS containing 0.5% BSA; 
    Isotype Control Antibody: Rabbit IgG/FITC(orange) ,used under the same conditions.

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    图标文献和实验
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      原因。这篇文章旨在探索用 AAV 基因疗法治疗由 NPHS2 基因突变引起的肾病综合征。 实验设计 AAV-LK03 和 AAV 2/9 的选择:研究者比较了 AAV-LK03 和 AAV 2/9 两种血清型在人类和鼠类足细胞中的转导效率。 体外实验:通过体外培养的突变人类足细胞中来测试基因疗法的效果。 体内实验:在诱导型足细胞蛋白(Podocin)敲除小鼠模型中测试疾病诱导前(预防性)的基因治疗效果,在诱导型突变 Podocin 敲入小鼠中测试疾病诱导后(治疗性)的基因疗法效果。 图 4 体内

    • Generation of Antibody Molecules Through Antibody Engineering

      been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional

    • The Antibody Molecule

      The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera

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