Mineralocorticoid receptor Polyclonal Antibody
规格: | / 60μL / 120μL / 200μL |
价格: | / ¥1380 / ¥2220 / ¥3300 |
货号:E-AB-70260
宿主: Rabbit
反应性: H
应用: WB
Overview
Synonyms | Aldosterone receptor,MCR,MGC133092,Mineralocorticoid receptor,MLR,MR,NR3 C2,NR3C2,NR3C2 protein,Nuclear receptor subfamily 3 group C member 2,Mineralocorticoid receptor抗体 |
Swissprot | P08235 |
Source | Rabbit |
Reactivity | Human |
Immunogen | KLH conjugated Synthetic peptide corresponding to Mouse Mineralocorticoid receptor |
Application | WB(Detection kit: E-IR-R304) |
Recommended dilution | WB,,1:500-1:2000; |
Concentration | 1.3 mg/mL |
Clonality | Polyclonal |
Properties
Cellular localization | Cytoplasm, Endoplasmic reticulum, Membrane, Nucleus |
Tissue specificity | Ubiquitous. Highly expressed in distal tubules, convoluted tubules and cortical collecting duct in kidney, and in sweat glands. Detected at lower levels in cardiomyocytes, in epidermis and in colon enterocytes. |
Isotype | IgG |
Purification | Affinity purification |
Conjugation | Unconjugated |
Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
Storage buffer | PBS with 0.02% sodium azide,100 μg/ml BSA and 50% glycerol. |
Background | This gene encodes the mineralocorticoid receptor, which mediates aldosterone actions on salt and water balance within restricted target cells. The protein functions as a ligand-dependent transcription factor that binds to mineralocorticoid response elements in order to transactivate target genes. Mutations in this gene cause autosomal dominant pseudohypoaldosteronism type I, a disorder characterized by urinary salt wasting. Defects in this gene are also associated with early onset hypertension with severe exacerbation in pregnancy. Alternative splicing results in multiple transcript variants. |