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Rabbit Polyclonal Anti-ACE1 antibody (STJ98743)
Supplier: St John’s Laboratory Ltd.
Recommended applications: IHC-P, ELISA
Recommended dilution: IHC-P 1:50-300; ELISA 1:5000-20000
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
|ACE 1 antibody|ACE antibody|ACE T antibody|ACE_HUMAN antibody|ACE1 antibody|Angiotensin converting enzyme somatic isoform antibody|Angiotensin converting enzyme testis specific isoform antibody|Angiotensin I converting enzyme 1 antibody|Angiotensin I converting enzyme antibody|Angiotensin I converting enzyme peptidyl dipeptidase A 1 antibody|angiotensin I converting enzyme peptidyl-dipeptidase A 1 transcript antibody|Angiotensin-converting enzyme antibody|Carboxycathepsin antibody|CD 143 antibody|CD143 antibody|CD143 antigen antibody|DCP 1 antibody|DCP antibody|DCP1 antibody|Dipeptidyl carboxypeptidase 1 antibody|Dipeptidyl carboxypeptidase I antibody|Kininase II antibody|MGC26566 antibody|MVCD3 antibody|Peptidase P antibody|Peptidyl dipeptidase A antibody|soluble form antibody|Testicular ECA antibody|Anti-Angiotensin Converting Enzyme 1 antibody [9B9] (ab77990)
SCBT cat No: sc-23908|sc-69994|sc-69993|sc-69991|sc-69992|sc-23909|sc-374198|sc-12187|sc-271860|sc-20791|sc-376132|sc-12184|
|Catalogue No.|| |
Anti-ACE1 antibody detects endogenous ACE1.
Synthetic peptide from human protein at AA range: 41-90.
|Recommended dilution|| |
IHC-P 1:50-300; ELISA 1:5000-20000
Anti-ACE1 antibody was tube-contained in PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.
Anti-ACE1 antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
ACE 1 antibody, ACE antibody, ACE T antibody, ACE_HUMAN antibody, ACE1 antibody, Angiotensin converting enzyme somatic isoform antibody, Angiotensin converting enzyme testis specific isoform antibody, Angiotensin I converting enzyme 1 antibody, Angiotensin I converting enzyme antibody, Angiotensin I converting enzyme peptidyl dipeptidase A 1 antibody, angiotensin I converting enzyme peptidyl-dipeptidase A 1 transcript antibody, Angiotensin-converting enzyme antibody, Carboxycathepsin antibody, CD 143 antibody, CD143 antibody, CD143 antigen antibody, DCP 1 antibody, DCP antibody, DCP1 antibody, Dipeptidyl carboxypeptidase 1 antibody, Dipeptidyl carboxypeptidase I antibody, Kininase II antibody, MGC26566 antibody, MVCD3 antibody, Peptidase P antibody, Peptidyl dipeptidase A antibody, soluble form antibody, Testicular ECA antibody
|Database links|| |
|Protein function|| |
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.
|Protein tissue specificity|| |
Ubiquitously expressed, with highest levels in lung, kidney, heart, gastrointestinal system and prostate. Isoform Testis-specific is expressed in spermatocytes and adult testis. .
|Involvement in disease|| |
Ischemic stroke (ISCHSTR) [MIM:601367]: 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. . Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.; Renal tubular dysgenesis (RTD) [MIM:267430]: 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). . Note=The disease is caused by mutations affecting the gene represented in this entry.; Microvascular complications of diabetes 3 (MVCD3) [MIM:612624]: Pathological conditions that develop in numerous tissues and organs as a consequence of diabetes mellitus. They include diabetic retinopathy, diabetic nephropathy leading to end-stage renal disease, and diabetic neuropathy. Diabetic retinopathy remains the major cause of new-onset blindness among diabetic adults. It is characterized by vascular permeability and increased tissue ischemia and angiogenesis. . Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.; Intracerebral hemorrhage (ICH) [MIM:614519]: A pathological condition characterized by bleeding into one or both cerebral hemispheres including the basal ganglia and the cerebral cortex. It is often associated with hypertension and craniocerebral trauma. Intracerebral bleeding is a common cause of stroke. . Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the peptidase M2 family.
|Protein post-translational modifications|| |
Phosphorylated by CK2 on Ser-1299; which allows membrane retention. .
|Protein cellular localization|| |
Angiotensin-converting enzyme, soluble form: Secreted.; Cell membrane; Single-pass type I membrane protein. Cytoplasm . Note=Detected in both cell membrane and cytoplasm in neurons. .
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St John’s Laboratory Ltd.
|Product type|| |
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