FITC标记的肾小球裂孔膜蛋白PDCN抗体

¥2980
LMAI Bio
中国/美国/欧洲
2021-08-05 12:00

上海联迈生物工程有限公司

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产品属性
供应商上海联迈生物工程有限公司
数量大量
靶点详见说明书
级别1
目录编号LM-6597R-FITC
克隆性多克隆
抗原来源Rabbit
保质期1年
抗体英文名Anti-NPHS2/Podocin/FITC
抗体名Anti-NPHS2/Podocin/FITC
标记物FITC标记
宿主Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,
适应物种Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit,
免疫原详见说明书
亚型IGg
形态粉末、液体、冻干粉
应用范围IF=1:50-200
浓度1mg/ml
保存条件-20 °C
规格100ul
产品说明
FITC标记的肾小球裂孔膜蛋白PDCN抗体
英文名称Anti-NPHS2/Podocin/FITC
中文名称FITC标记的肾小球裂孔膜蛋白PDCN抗体
别 名nephrosis 2, idiopathic, steroid resistant; NPHS2 gene; PDCN; Podocin; SRN1; PODO_HUMAN.
Journal
PMID
IF
Application
Biology of Sex Differences (2015)
25729563
4.8400
FCM
规格价格100ul/2980元 购买 大包装/询价
说 明 书100ul
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IF=1:50-200
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
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.
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.

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.