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ACE1 Monoclonal Antibody

Monoclonal antibody

Specification

BYab-02343

  • 50UL $180 100UL $255
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Product introduction>

Host
Reactiveness
Use
Molecular weight (DA)
Immunogen
Purified recombinant human ACE1 (N-terminus) protein fragments expressed in E.coli.
Specificity
ACE1 Monoclonal Antibody detects endogenous levels of ACE1 protein.
Source
Monoclonal, Mouse
Formulation
Purified mouse monoclonal in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50% glycerol.
Dilution rate
Western Blot: 1/1000 - 1/2000. Not yet tested in other applications.
Purification process (Immunogen)
Affinity purification
Concentration
1 mg/ml
Background
This 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. Multiple alternatively spliced transcript variants encoding different isoforms have been identified, and two most abundant spliced variants encode the somatic form and the testicular form, respectively, that are equally active. [provided by RefSeq, May 2010],
Function
catalytic activity:Release of a C-terminal dipeptide, oligopeptide-|-Xaa-Yaa, when Xaa is not Pro, and Yaa is neither Asp nor Glu. Thus, conversion of angiotensin I to angiotensin II, with increase in vasoconstrictor activity, but no action on angiotensin II.,cofactor:Binds 2 zinc ions per subunit. The Testis-specific isoform only binds 1 zinc ion per subunit.,cofactor:Binds 3 chloride ions per subunit.,disease: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).,disease:Genetic variations in ACE could influence susceptibility to diabetic nephropathy [MIM:612624]; also called susceptibility to microvascular complications of diabetes type 3
Gene Name
ACE
Protein name
Angiotensin-converting enzyme
Abbreviation
ACE
Other name
ACE; DCP; DCP1; Angiotensin-converting enzyme; ACE; Dipeptidyl carboxypeptidase I; Kininase II; CD antigen CD143
Fields
>>Renin-angiotensin system;>>Renin secretion;>>Chagas disease;>>Coronavirus disease - COVID-19;>>Hypertrophic cardiomyopathy;>>Diabetic cardiomyopathy
Human gene ID
1636
Human protein sequence Database
P12821
Mouse gene ID
11421
Mouse protein sequence database
P09470
Rat gene ID
24310
Rat protein sequence database
P47820
Cellular localization
[Angiotensin-converting enzyme, soluble form]: Secreted.; Cell membrane; Single-pass type I membrane protein. Cytoplasm . Detected in both cell membrane and cytoplasm in neurons. .
Tissue expression
Ubiquitously expressed, with highest levels in lung, kidney, heart, gastrointestinal system and prostate. Isoform Testis-specific is expressed in spermatocytes and adult testis.
Storage
-20°C/1 year

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ACE1 Monoclonal Antibody

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