Analytical Data
-
基因名
Kirrel1/NEPH1
-
简介
The Kirrel1/NEPH1 protein is essential for the normal function of the glomerular filtration barrier in the kidney, maintaining stable podocyte structure through finger-like foot processes and gap septal cell-cell junctions. As a signaling molecule, it requires TEC kinase to fully activate the transcription factor AP-1. Kirrel1/NEPH1 Protein, Human (HEK293, His) is the recombinant human-derived Kirrel1/NEPH1 protein, expressed by HEK293 , with C-His labeled tag.
- Application
-
别名
Kin of IRRE-like protein 1; Kin of irregular chiasm-like protein 1; Nephrin-like protein 1; Kirrel1; Neph1
-
种属
Human
-
表达系统
HEK293
-
标签
C-His
-
纯度
Greater than 90% as determined by SDS-PAGE.
-
蛋白编号
Q96J84-1
-
表达区间
Q17-L493
-
蛋白长度
Partial
-
分子量
53.5 kDa.
-
内毒素
< 1.0 EU per μg protein as determined by the LAL method.
-
性状
Freeze-dried powder
-
缓冲液
PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.
-
复溶方法
Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.
- 个性化定制
-
稳定性测试
The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.
-
保存条件 & 期限
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
-
运输条件
In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.
Quality inspection process
Related Products
Protein Description
Kirrel1, also known as Nephrin-like protein 1 (NEPH1), is a member of the immunoglobulin superfamily that plays a pivotal role in the development and maintenance of the kidney's filtration barrier. Its significance became apparent through studies linking mutations in the Kirrel1/NEPH1 gene to congenital nephrotic syndrome, a condition characterized by proteinuria and edema due to the faulty filtration process in the kidneys. Research on Kirrel1/NEPH1 focuses on understanding its molecular mechanisms in podocyte biology—the specialized cells that form part of the glomerular filtration barrier. The protein is known to participate in cell-cell adhesion and signaling pathways that contribute to podocyte stability and function. Given its critical role in kidney health, Kirrel1/NEPH1 is a target of interest for therapeutic development in kidney diseases. Studies involving recombinant Kirrel1/NEPH1 proteins aim to elucidate its structural properties, interaction with other proteins, and potential functions in cellular signaling. Investigating Kirrel1/NEPH1 may provide insights into novel approaches for treating kidney disorders, as well as improve our understanding of the underlying pathophysiological processes in renal diseases. The ongoing research in this area not only enhances our knowledge of kidney biology but also paves the way for the development of innovative strategies to combat kidney-related ailments.
