Rabbit anti-Human NPHP1 Monoclonal Antibody-单克隆抗体-北京百欧泰生物科技有限公司

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抗体产品
- 一抗
  - --|--|流式抗体
  - --|--|单克隆抗体
  - --|--|重组兔单抗
  - --|--|多克隆抗体
  - --|--|小分子抗原抗体
  - --|--|抗体对
  - --|--|标签抗体
  - --|--|修饰性抗体
  - --|--|其他抗体
- 二抗
- 试剂盒
  - --|--|标记试剂盒
  - --|--|其他试剂盒
  - --|--|标记染料
蛋白产品
生物材料
- 金属纳米材料
  - --|--|金纳米球
  - --|--|金纳米棒
  - --|--|银纳米球
  - --|--|金纳米海胆
  - --|--|碳纳米颗粒
  - --|--|特殊纳米颗粒
- 磁性微球
  - --|--|PS磁性微球
  - --|--|SiO2磁性微球
  - --|--|Fe3O4磁性微球
  - --|--|功能化磁性微球
  - --|--|Magnetic Particles Conjugates
  - --|--|琼脂糖磁性微球
  - --|--|磁性微球试剂盒
  - --|--|Fe2O3磁性微球
  - --|--|脲醛树脂UF磁性微球
  - --|--|其他磁性微球
- 单分散微球
  - --|--|聚苯乙烯微球
  - --|--|二氧化硅微球
  - --|--|PMMA微球
  - --|--|PET微球
  - --|--|PVA微球
  - --|--|PVC微球
  - --|--|PP微球
  - --|--|PE微球
  - --|--|GMA微球
  - --|--|聚乳酸PLA微球
  - --|--|PLGA微球
  - --|--|聚左旋乳酸PLLA微球
  - --|--|聚右旋乳酸PDLA微球
  - --|--|聚己内酯PCL微球
  - --|--|PTFE聚四氟乙烯微球
  - --|--|聚丁二酸丁二醇酯PBS微球
- 其他材料
  - --|--|上转换纳米颗粒
  - --|--|量子点
  - --|--|荧光微球
  - --|--|色谱填料
热销产品
- 猴痘相关产品
- 新冠相关产品
- 外泌体相关产品
- 常用试剂
  - --|--|转染试剂
  - --|--|ELISA-FCM试剂
  - --|--|WB试剂
  - --|--|IHC-ICC-IF试剂
  - --|--|载体材料

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Rabbit anti-Human NPHP1 Monoclonal Antibody

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Documentation
Citations

Cat No	BMA-2494
Conjugate
Type	重组兔多抗
Source	Rabbit
Size	50 uL
Application	WB
Format	Liquid
Concentration	Please refer to the vial lable for the specific concentration.
Buffer	Supplied in PBS with 0.02% sodium azide,50% glycerol,pH7.3.
Species	Human
Storage	Store at -20℃. Avoid freeze / thaw cycles.
Synonyms	NPHP1;JBTS4;NPH1;SLSN1
Purification	Affinity purification
MolecularWeight	83kDa
Description
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 different isoforms have been found for this gene.

We can offer labeled proteins/antibodies using a broad range of intensely fluorescent dyes and labels including FITC, Biotin, Alexa Fluor, Rhodamine B, Cy, Co-Au.

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单克隆抗体

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Rabbit anti-Human NPHP1 Monoclonal Antibody