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AG330 PER1 (Hu), control peptide for AB5424P

PER1 (Hu), control peptide for AB5424P : FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.
Research Category: Neuroscience Research Sub-Category: Circadian Rhythm & Sleep Gene Symbol: ACE, DCP, ACE1, DCP1, carboxycathepsin, ACE-T, MGC26566, CD143, EC 3.4.15.1, EC 3.2.1.- [Contains: Angiotensin-converting enzyme, testis- specific isoform, soluble form]., EC 3.4.15.1 [Contains: Angiotensin-converting enzyme, somatic isoform, soluble form]. UniProt Number: P22966
AG330
100 µg  
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      Description
      Catalogue NumberAG330
      Brand Family Chemicon®
      Trade Name
      • Chemicon
      DescriptionPER1 (Hu), control peptide for AB5424P
      OverviewPeptide from human Per1.
      References
      Product Information
      PresentationLiquid in PBS, pH 7.
      Quality LevelMQ300
      Applications
      Key Applications
      • Cell Function Assay
      Application NotesFor use in blocking the reactivity of AB5424P.

      Optimal working dilution must be determined by the end user.
      Biological Information
      Concentration1.0 mg/mL
      Entrez Gene Number
      Entrez Gene SummaryThis gene encodes an enzyme involved in catalyzing the conversion of angiotensin I into a physiologically active peptide angiotensin II. Angiotensin II is a potent vasopressor and aldosterone-stimulating peptide that controls blood pressure and fluid-electrolyte balance. This enzyme plays a key role in the renin-angiotensin system. Many studies have associated the presence or absence of a 287 bp Alu repeat element in this gene with the levels of circulating enzyme or cardiovascular pathophysiologies. Two most abundant alternatively spliced variants of this gene encode two isozymes - the somatic form and the testicular form that are equally active. Multiple additional alternatively spliced variants have been identified but their full length nature has not been determined.
      Gene Symbol
      • ACE
      • DCP
      • ACE1
      • DCP1
      • carboxycathepsin
      • ACE-T
      • MGC26566
      • CD143
      • EC 3.4.15.1
      • EC 3.2.1.- [Contains: Angiotensin-converting enzyme, testis- specific isoform, soluble form].
      • EC 3.4.15.1 [Contains: Angiotensin-converting enzyme, somatic isoform, soluble form].
      UniProt Number
      UniProt SummaryFUNCTION: SwissProt: P22966 # Converts angiotensin I to angiotensin II by release of the terminal His-Leu, this results in an increase of the vasoconstrictor activity of angiotensin. Also able to inactivate bradykinin, a potent vasodilator. Has also a glycosidase activity which releases GPI-anchored proteins from the membrane by cleaving the mannose linkage in the GPI moiety.| P12821 # Converts angiotensin I to angiotensin II by release of the terminal His-Leu, this results in an increase of the vasoconstrictor activity of angiotensin. Also able to inactivate bradykinin, a potent vasodilator.
      COFACTOR: Binds 1 zinc ion per subunit. & Binds 2 chloride ions per subunit.
      SIZE: 732 amino acids; 83330 Da
      SUBCELLULAR LOCATION: Angiotensin-converting enzyme, testis- specific isoform, soluble form: Secreted. & Cell membrane; Single-pass type I membrane protein.
      TISSUE SPECIFICITY: Spermatocytes, adult testis.
      DOMAIN: SwissProt: P22966
      PTM: Phosphorylated by CK2 on Ser-725; which allows membrane retention (By similarity).
      DISEASE: SwissProt: P12821 # Genetic variations in ACE may be a cause of susceptibility to ischemic stroke [MIM:601367]; also known as cerebrovascular accident or cerebral infarction. A stroke is an acute neurologic event leading to death of neural tissue of the brain and resulting in loss of motor, sensory and/or cognitive function. Ischemic strokes, resulting from vascular occlusion, is considered to be a highly complex disease consisting of a group of heterogeneous disorders with multiple genetic and environmental risk factors. & Defects in ACE are a cause of renal tubular dysgenesis (RTD) [MIM:267430]. RTD is an autosomal recessive severe disorder of renal tubular development characterized by persistent fetal anuria and perinatal death, probably due to pulmonary hypoplasia from early-onset oligohydramnios (the Potter phenotype). & Genetic variations in ACE can influence susceptibility to diabetic nephropathy [MIM:603933]. Diabetic nephropathy is a kidney disease and resultant kidney function impairment due to the long standing effects of diabetes on the microvasculature (glomerulus) of the kidney. Features include increased urine protein and declining kidney function.
      SIMILARITY: SwissProt: P22966 ## Belongs to the peptidase M2 family.| P12821 ## Belongs to the peptidase M2 family.
      MISCELLANEOUS: The glycosidase activity probably uses different active site residues than the metalloprotease activity. & Inhibitors of ACE are commonly used to treat hypertension and cardiac dysfunction.
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Usage Statement
      • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
      Storage and Shipping Information
      Storage ConditionsMaintain at -20°C in undiluted aliquots for up to 6 months after date of receipt. Avoid repeated freeze/thaw cycles.
      Packaging Information
      Material Size100 µg
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Référence GTIN
      AG330 04053252403095