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AB39172

Anti-Angiotensin Converting Enzyme 1 antibody

4

(1 Review)

|

(8 Publications)

Rabbit Polyclonal Angiotensin Converting Enzyme 1 antibody. Suitable for WB and reacts with Recombinant fragment samples. Cited in 8 publications. Immunogen corresponding to Synthetic Peptide within Human ACE.

View Alternative Names

CD143, DCP, DCP1, ACE, Angiotensin-converting enzyme, Dipeptidyl carboxypeptidase I, Kininase II

1 Images
Western blot - Anti-Angiotensin Converting Enzyme 1 antibody (AB39172)
  • WB

Unknown

Western blot - Anti-Angiotensin Converting Enzyme 1 antibody (AB39172)

All lanes:

Western blot - Anti-Angiotensin Converting Enzyme 1 antibody (ab39172) at 1/1000 dilution

Lane 1:

ACE1 at 0.05 µg

Lane 2:

ACE1 at 0.01 µg

Lane 3:

ACE1 at 0.001 µg

Predicted band size: 150 kDa

Observed band size: 170 kDa

false

Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Applications

WB

applications

Immunogen

Synthetic Peptide within Human ACE. The exact immunogen used to generate this antibody is proprietary information.

P12821

Specificity

This antibody is specific for Angiotensin Converting Enzyme 1.

Reactivity data

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AB239703

ACE Assay Kit (Angiotensin I Converting Enzyme)

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We recommend this product because it’s often used in the same experiment or related research.

We advise that you always check the datasheet to ensure it fits your experiments, or contact ourtechnical teamfor help.

Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Purification notes
This antibody has been peptide-affinity purified.
Storage buffer
Preservative: 0.05% Sodium azide Constituents: 50% Glycerol (glycerin, glycerine)
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Angiotensin Converting Enzyme 1 also known as ACE1 or ACE is an important enzyme in the renin-angiotensin system. This enzyme exhibits a significant role in blood pressure regulation. ACE1 is a zinc-metallopeptidase with a molecular weight of approximately 130 kDa. It converts angiotensin I into the potent vasoconstrictor angiotensin II a critical function in cardiovascular physiology. ACE1 is widely expressed in endothelial cells particularly in the lungs kidneys and the small intestine.
Biological function summary

The enzyme generates angiotensin II by cleaving angiotensin I. Angiotensin II an important effector peptide impacts cardiovascular and renal systems influencing vasoconstriction and fluid balance. While not directly forming a complex ACE1's activity increases the potency of angiotensin II which binds to angiotensin II receptors to exert its effects therefore indirectly forming a functional signaling complex.

Pathways

ACE1 plays a central role in the renin-angiotensin system and the kallikrein-kinin system. The enzyme's activity boosts angiotensin II production which connects it to the regulation of blood pressure via the renin-angiotensin pathway. ACE1 also indirectly interacts with proteins like bradykinin by degrading them modulating kinin-related functions and influencing inflammation and tension in vascular smooth muscle.

Understanding ACE1 is important for addressing hypertension and congestive heart failure. ACE1's conversion of angiotensin I to angiotensin II means overactivity can cause elevated blood pressure leading to hypertension. This makes ACE inhibitors such as lisinopril and ramipril therapeutic for these conditions. Furthermore its connection with aldosterone production places ACE1 in relevance to heart failure as excessive aldosterone can cause detrimental remodeling of cardiac tissue.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

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 : 15615692, PubMed : 20826823, PubMed : 2558109, PubMed : 4322742, PubMed : 7523412, PubMed : 7683654). Composed of two similar catalytic domains, each possessing a functional active site, with different selectivity for substrates (PubMed : 10913258, PubMed : 1320019, PubMed : 1851160, PubMed : 19773553, PubMed : 7683654, PubMed : 7876104). 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 : 11432860, PubMed : 1851160, PubMed : 19773553, PubMed : 23056909, PubMed : 4322742). Also able to inactivate bradykinin, a potent vasodilator, and therefore enhance the blood pressure response (PubMed : 15615692, PubMed : 2558109, PubMed : 4322742, PubMed : 6055465, PubMed : 6270633, PubMed : 7683654). Acts as a regulator of synaptic transmission by mediating cleavage of neuropeptide hormones, such as substance P, neurotensin or enkephalins (PubMed : 15615692, PubMed : 6208535, PubMed : 6270633, PubMed : 656131). Catalyzes degradation of different enkephalin neuropeptides (Met-enkephalin, Leu-enkephalin, Met-enkephalin-Arg-Phe and possibly Met-enkephalin-Arg-Gly-Leu) (PubMed : 2982830, PubMed : 6270633, PubMed : 656131). 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 (By similarity). Met-enkephalin-Arg-Phe cleavage by ACE decreases activation of OPRM1, leading to long-term synaptic potentiation of glutamate release (By similarity). Also acts as a regulator of hematopoietic stem cell differentiation by mediating degradation of hemoregulatory peptide N-acetyl-SDKP (AcSDKP) (PubMed : 26403559, PubMed : 7876104, PubMed : 8257427, PubMed : 8609242). Acts as a regulator of cannabinoid signaling pathway by mediating degradation of hemopressin, an antagonist peptide of the cannabinoid receptor CNR1 (PubMed : 18077343). Involved in amyloid-beta metabolism by catalyzing degradation of Amyloid-beta protein 40 and Amyloid-beta protein 42 peptides, thereby preventing plaque formation (PubMed : 11604391, PubMed : 16154999, PubMed : 19773553). Catalyzes cleavage of cholecystokinin (maturation of Cholecystokinin-8 and Cholecystokinin-5) and Gonadoliberin-1 (both maturation and degradation) hormones (PubMed : 10336644, PubMed : 2983326, PubMed : 7683654, PubMed : 9371719). 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 : 10336644, PubMed : 19773553, PubMed : 7876104).. Angiotensin-converting enzyme, soluble form. Soluble form that is released in blood plasma and other body fluids following proteolytic cleavage in the juxtamembrane stalk region.. Isoform Testis-specific. Isoform produced by alternative promoter usage that is specifically expressed in spermatocytes and adult testis, and which is required for male fertility (PubMed : 1651327, PubMed : 1668266). In contrast to somatic isoforms, only contains one catalytic domain (PubMed : 1651327, PubMed : 1668266). Acts as a dipeptidyl carboxypeptidase that removes dipeptides from the C-terminus of substrates (PubMed : 1668266, PubMed : 24297181). The identity of substrates that are needed for male fertility is unknown (By similarity). May also have a glycosidase activity which releases GPI-anchored proteins from the membrane by cleaving the mannose linkage in the GPI moiety. The GPIase activity was reported to be essential for the egg-binding ability of the sperm (By similarity). This activity is however unclear and has been challenged by other groups, suggesting that it may be indirect (By similarity).
See full target information ACE

Publications (8)

Recent publications for all applications. Explore the full list and refine your search

Cytotechnology 73:745-754 PubMed34493899

2021

Pulmonary AngII promotes LPS-induced lung inflammation by regulating microRNA-143.

Applications

Unspecified application

Species

Unspecified reactive species

Shenglan Wang,Yan Tan,Tingting Yang,Chen Liu,Rufang Li

Frontiers in physiology 12:642274 PubMed33868005

2021

Diuretic Action of Apelin-13 Mediated by Inhibiting cAMP/PKA/sPRR Pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Yanting Chen,Chuanming Xu,Jiajia Hu,Mokan Deng,Qixiang Qiu,Shiqi Mo,Yanhua Du,Tianxin Yang

BMC physiology 15:2 PubMed25971747

2015

Antenatal maternal low protein diet: ACE-2 in the mouse lung and sexually dimorphic programming of hypertension.

Applications

Unspecified application

Species

Unspecified reactive species

Ravi Goyal,Jonathan Van-Wickle,Dipali Goyal,Lawrence D Longo

American journal of physiology. Cell physiology 307:C1093-101 PubMed25273883

2014

Induction of angiotensin-converting enzyme after miR-143/145 deletion is critical for impaired smooth muscle contractility.

Applications

Unspecified application

Species

Unspecified reactive species

Diana Dahan,Mari Ekman,Anna-Karin Larsson-Callerfelt,Karolina Turczyńska,Thomas Boettger,Thomas Braun,Karl Swärd,Sebastian Albinsson

Journal of the renin-angiotensin-aldosterone system : JRAAS 14:137-45 PubMed22898440

2012

Antenatal maternal protein deprivation: sexually dimorphic programming of the pancreatic renin-angiotensin system.

Applications

Unspecified application

Species

Unspecified reactive species

Ravi Goyal,Christine Wong,Jonathan Van Wickle,Lawrence D Longo

Placenta 32:134-9 PubMed21130492

2010

Antenatal maternal hypoxic stress: adaptations of the placental renin-angiotensin system in the mouse.

Applications

Unspecified application

Species

Unspecified reactive species

R Goyal,R Lister,A Leitzke,D Goyal,C P Gheorghe,L D Longo

Reproductive sciences (Thousand Oaks, Calif.) 18:180-9 PubMed20978179

2010

Antenatal maternal hypoxic stress: adaptations in fetal lung Renin-Angiotensin system.

Applications

Unspecified application

Species

Unspecified reactive species

Ravi Goyal,Arthur Leitzke,Dipali Goyal,Ciprian P Gheorghe,Lawrence D Longo

The Journal of clinical investigation 119:2634-47 PubMed19690389

2009

Acquisition of the contractile phenotype by murine arterial smooth muscle cells depends on the Mir143/145 gene cluster.

Applications

WB

Species

Mouse

Thomas Boettger,Nadine Beetz,Sawa Kostin,Johanna Schneider,Marcus Krüger,Lutz Hein,Thomas Braun
View all publications

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