Mouse ACE ELISA Kit is a single-wash 90-min SimpleStep ELISA® for the quantitative measurement of Mouse ACE in Cell culture media, Heparin Plasma, Citrate plasma, Cell culture supernatant, Serum, EDTA Plasma samples.
Colorimetric
Cell culture media, Heparin Plasma, Citrate plasma, Cell culture supernatant, Serum, EDTA Plasma
Sandwich (quantitative)
Mouse
46.88 - 3000 pg/mL
1h 30m
= 24 pg/mL
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application sELISA | Reactivity Reacts | Dilution info - | Notes - |
Select an associated product type
Dipeptidyl carboxypeptidase that removes dipeptides from the C-terminus of a variety of circulating hormones, such as angiotensin I, bradykinin or enkephalins, thereby playing a key role in the regulation of blood pressure, electrolyte homeostasis or synaptic plasticity (PubMed:11723129, PubMed:12777443, PubMed:14757757, PubMed:16270063, PubMed:35201898, PubMed:7753170, PubMed:8642790, PubMed:9231832). Composed of two similar catalytic domains, each possessing a functional active site, with different selectivity for substrates (PubMed:11303049). Plays a major role in the angiotensin-renin system that regulates blood pressure and sodium retention by the kidney by converting angiotensin I to angiotensin II, resulting in an increase of the vasoconstrictor activity of angiotensin (PubMed:11303049, PubMed:14757757, PubMed:9231832). Also able to inactivate bradykinin, a potent vasodilator, and therefore enhance the blood pressure response (By similarity). Acts as a regulator of synaptic transmission by mediating cleavage of neuropeptide hormones, such as substance P, neurotensin or enkephalins (By similarity). Catalyzes degradation of different enkephalin neuropeptides (Met-enkephalin, Leu-enkephalin, Met-enkephalin-Arg-Phe and possibly Met-enkephalin-Arg-Gly-Leu) (PubMed:35201898). Acts as a regulator of synaptic plasticity in the nucleus accumbens of the brain by mediating cleavage of Met-enkephalin-Arg-Phe, a strong ligand of Mu-type opioid receptor OPRM1, into Met-enkephalin (PubMed:35201898). Met-enkephalin-Arg-Phe cleavage by ACE decreases activation of OPRM1, leading to long-term synaptic potentiation of glutamate release (PubMed:35201898). Also acts as a regulator of hematopoietic stem cell differentiation by mediating degradation of hemoregulatory peptide N-acetyl-SDKP (AcSDKP) (PubMed:11303049). Acts as a regulator of cannabinoid signaling pathway by mediating degradation of hemopressin, an antagonist peptide of the cannabinoid receptor CNR1 (By similarity). Involved in amyloid-beta metabolism by catalyzing degradation of Amyloid-beta protein 40 and Amyloid-beta protein 42 peptides, thereby preventing plaque formation (By similarity). Catalyzes cleavage of cholecystokinin (maturation of Cholecystokinin-8 and Cholecystokinin-5) and Gonadoliberin-1 (both maturation and degradation) hormones (By similarity). Degradation of hemoregulatory peptide N-acetyl-SDKP (AcSDKP) and amyloid-beta proteins is mediated by the N-terminal catalytic domain, while angiotensin I and cholecystokinin cleavage is mediated by the C-terminal catalytic region (PubMed:11303049).Angiotensin-converting enzyme, soluble formSoluble form that is released in blood plasma and other body fluids following proteolytic cleavage in the juxtamembrane stalk region.Isoform Testis-specificIsoform produced by alternative promoter usage that is specifically expressed in spermatocytes and adult testis, and which is required for male fertility (PubMed:1651914, PubMed:9482924). In contrast to somatic isoforms, only contains one catalytic domain (PubMed:16270063). Acts as a dipeptidyl carboxypeptidase that removes dipeptides from the C-terminus of substrates (PubMed:16270063). The identity of substrates that are needed for male fertility is unknown (PubMed:16270063). Isoform Testis-specific and isoform Somatic have distinct activities and cannot completely compensate for the loss of the other when expressed in somatic tissues or testis (PubMed:10831599, PubMed:11723129, PubMed:12777443, PubMed:16270063, PubMed:9664078). May also have a glycosidase activity which releases GPI-anchored proteins from the membrane by cleaving the mannose linkage in the GPI moiety (PubMed:15665832). The GPIase activity was reported to be essential for the egg-binding ability of the sperm (PubMed:15665832). This activity is however unclear and has been challenged by other groups, suggesting that it may be indirect (PubMed:16270063).
CD143, Dcp1, Ace, Angiotensin-converting enzyme, ACE, Dipeptidyl carboxypeptidase I, Kininase II
Mouse ACE ELISA Kit is a single-wash 90-min SimpleStep ELISA® for the quantitative measurement of Mouse ACE in Cell culture media, Heparin Plasma, Citrate plasma, Cell culture supernatant, Serum, EDTA Plasma samples.
Colorimetric
Cell culture media, Heparin Plasma, Citrate plasma, Cell culture supernatant, Serum, EDTA Plasma
Sandwich (quantitative)
Mouse
46.88 - 3000 pg/mL
1h 30m
Pre-coated microplate (12 x 8 well strips)
= 24 pg/mL
Sample | n | mean | SD | C.V. |
---|---|---|---|---|
Sample Serum | n 8 | mean - | SD - | C.V. 2.6 |
Sample | n | mean | SD | C.V. |
---|---|---|---|---|
Sample Serum | n 3 | mean - | SD - | C.V. 1 |
Sample type | Average % | Range |
---|---|---|
Sample type Cell culture supernatant | Average % = 104 | Range 98 - 119 % |
Sample type Serum | Average % = 83 | Range 77 - 93 % |
Sample type EDTA Plasma | Average % = 104 | Range 90 - 122 % |
Sample type Cell culture media | Average % = 88 | Range 84 - 93 % |
Sample type Heparin Plasma | Average % = 106 | Range 102 - 114 % |
Sample type Citrate plasma | Average % = 122 | Range 104 - 141 % |
Blue Ice
+4°C
+4°C
+4°C
Mouse ACE ELISA Kit (ab256400) is a single-wash 90 min sandwich ELISA designed for the quantitative measurement of ACE protein in cell culture media, cell culture supernatant, cit plasma, edta plasma, hep plasma, and serum. It uses our proprietary SimpleStep ELISA® technology. Quantitate Mouse ACE with 24 pg/ml sensitivity.
SimpleStep ELISA® technology employs capture antibodies conjugated to an affinity tag that is recognized by the monoclonal antibody used to coat our SimpleStep ELISA® plates. This approach to sandwich ELISA allows the formation of the antibody-analyte sandwich complex in a single step, significantly reducing assay time. See the SimpleStep ELISA® protocol summary in the image section for further details. Our SimpleStep ELISA® technology provides several benefits:
- Single-wash protocol reduces assay time to 90 minutes or less
- High sensitivity, specificity and reproducibility from superior antibodies
- Fully validated in biological samples
- 96-wells plate breakable into 12 x 8 wells strips
A 384-well SimpleStep ELISA® microplate (Pre-coated 384 well Microplate SimpleStep ELISA® ab203359) is available to use as an alternative to the 96-well microplate provided with SimpleStep ELISA® kits.
ACE (Angiotensin-converting enzyme) converts angiotensin I to angiotensin II by release of the terminal His-Leu dipeptide, this results in an increase of the vasoconstrictor activity of angiotensin. It is also able to inactivate bradykinin, a potent vasodilator. ACE has also a glycosidase activity which releases GPI-anchored proteins from the membrane by cleaving the mannose linkage in the GPI moiety. This GPIase activity seems to be crucial for the egg-binding ability of the sperm.
This supplementary information is collated from multiple sources and compiled automatically.
Angiotensin Converting Enzyme 1 (ACE) also called peptidyl-dipeptidase A is a critical enzyme with a mass of approximately 150-180 kDa. It is mainly expressed in the lungs kidneys and endothelial cells. Mechanically ACE converts angiotensin I to angiotensin II by removing a dipeptide. This conversion is significant in the regulation of blood pressure. ACE also degrades bradykinin a peptide that causes blood vessels to dilate which further affects cardiovascular functions.
ACE is deeply involved in cardiovascular homeostasis and fluid balance. As a zinc metalloprotease it acts at the intersection of important physiological processes. It does not operate directly as part of a complex but interacts dynamically with substrates like angiotensin I and bradykinin. ACE activity results in the production of angiotensin II a potent vasoconstrictor which plays a role in blood pressure regulation and has effects on the electrolyte balance in the body.
ACE holds a central role in the renin-angiotensin system (RAS) and kinin-kallikrein system. In the RAS pathway it transforms angiotensin I into angiotensin II which directly impacts blood pressure regulation through vasoconstriction. Angiotensin II also influences the secretion of aldosterone from the adrenal cortex modulating electrolyte and fluid balance. Additionally ACE modulates the kinin-kallikrein system by degrading bradykinin which influences vasodilation and inflammation.
ACE has implications in hypertension and heart failure. Dysregulation of ACE activity contributes significantly to these conditions by altering levels of angiotensin II and bradykinin. Angiotensin II's role in vasoconstriction and inflammation ties ACE to the pathology of hypertension. In heart failure altered RAS activity including ACE function can exacerbate disease progression. Related proteins such as angiotensinogen and the angiotensin II type 1 receptor (AT1R) are directly involved in these disorders outlining the interconnected nature of ACE within these pathophysiological contexts.
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Example of mouse ACE standard curve in Sample Diluent NS.
The ACE standard curve was prepared as described in Section 10. Raw data values are shown in the table. Background-subtracted data values (mean +/- SD) are graphed.
Interpolated concentrations of native ACE in mouse serum and plasma samples.
The concentrations of ACE were measured in duplicates, interpolated from the ACE standard curves and corrected for sample dilution. Undiluted samples are as follows: serum 1:400, plasma (citrate) 1:400, plasma (EDTA) 1:400 and plasma (heparin) 1:400. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean ACE concentration was determined to be 928 ng/mL in neat serum, 762 ng/mL in neat plasma (citrate), 763 ng/mL in neat plasma (EDTA)and 901 ng/mL in neat plasma (heparin).
Interpolated concentrations of native ACE in mouse kidney tissue culture supernatant sample.
The concentrations of ACE were measured in duplicates, interpolated from the ACE standard curves and corrected for sample dilution. Undiluted samples are as follows: kidney tissue culture supernatant 25%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean ACE concentration was determined to be 61 ng/mL in neat kidney tissue culture supernatant.
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