| 영문 | albumin | 한글 | 알부민 |
|---|---|---|---|
| 설명 | 1.물에 녹을 수 있고 녹은 후에 열을 가하면 변성을 일으키는 모든 단백질의 총칭. 2.혈청 알부민의 의미로 쓰인다. 혈청이란 피를 뽑아 방치했을 경우에 혈액응고가 되고 난 뒤에 남아있는 맑은 액을 말하는 데 이곳에 녹아있는 사람의 단백질을 혈청 단백질이라고 하고 이 혈청단백질의 대부분(60%)을 차지하는 것이 알부민이다. 이 알부민의 기능은 우선 혈액속에 있는 여러 가지 호르몬 등의 물질과 결합하여 그 물질의 분해를 막고 다른 곳으로 이동시키는 역할과 혈액의 삼투압을 유지하는 일을 한다. |
||
| IED | inherited epidermal dysplasia; intermittent explosive disorder |
|---|---|
| HSA | Hazardous Substances Act; Health Services Administration; health systems agency; hereditary siderobl... |
| AER | Albumin Excretion Rate |
| A/G ratio | Albumin/Globulin ratio; 알부민대 글로불린의 비율 |
| Alb. | Albumin |
| MIDD | Maternally Inherited Diabetes and Deafness |
|---|---|
| 125I-BSA | 125 bovine serum albumin |
| BSA | 125)I-bovine serum albumin |
| HSA | 99m)Tc-human serum albumin |
| MAA | 99m)Tc-macroaggregated albumin |
| inherited albumin variants | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
|---|
| L-phase variants | Bacterial variant's which do not have rigid cell walls but which may contain varying amounts of cell wall material; they are spherical to coccobacillary in shape and vary in size from small bodies that pass through filters which retain bacteria to bodies that are larger than the bacterial form; they are Gram-negative and resistant to penicillin; some revert to the bacterial phase upon removal of the inducing substance, whereas others do not; the variant's differ greatly from the parent bacterial cells in mode of reproduction, physiology, growth requirements, and individual and colonial morphology; they are generally considered to be nonpathogenic, even if derived from a pathogenic bacterium. Origin: L. Fr. Lister Institute (05 Mar 2000) |
|---|---|
| dominantly inherited Levi's disease | Dwarfism characterised by low birth weight, snub nose, and stocky build; autosomal dominant inheritance. There is a similar autosomal recessive phenotype. Synonym: dominantly inherited Levi's disease. (05 Mar 2000) |
| inherited | Derived from a preformed genetic code present in the parents. Contrast with acquired. (05 Mar 2000) |
| inherited character | A single attribute of an animal or plant that is transmitted at one locus from generation to generation in accordance with Mendel's law. See: gene. Synonym: unit character. (05 Mar 2000) |
| acetosoluble albumin | A substance resembling serum albumin, but soluble in acetic acid. Synonym: acetosoluble albumin. (05 Mar 2000) |
| albumin | 1. <chemistry> Any protein that is soluble in water and moderately concentrated salt solutions and is coagulable by heat. Found in egg whites, blood, lymph, and other tissues and fluids. 2. <biochemistry> Serum albumin, the major plasma protein (approximately 60 per cent of the total), which is responsible for much of the plasma colloidal osmotic pressure and serves as a transport protein carrying large organic anions, such as fatty acids, bilirubin and many drugs and also carrying certain hormones, such as cortisol and thyroxine, when their specific binding globulins are saturated. Albumin is synthesised in the liver. Low serum levels occur in protein malnutrition, active inflammation and serious hepatic and renal disease. (31 Jan 2000) |
| albumin A | The normal or common type of human serum albumin. (05 Mar 2000) |
| albumin B | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin Ghent | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin-globulin ratio | The ratio of albumin to globulin in the serum or in the urine in kidney disease; the normal ratio in the serum is approximately 1.55. (05 Mar 2000) |
| albumin Mexico | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin Naskapi | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin Reading | Types of human serum albumin, distinguished by characteristic mobility patterns on electrophoresis; each type is due to a mutation of a gene controlling albumin synthesis; the mutant genes are codominant with the normal gene for albumin A, and the group forms a system of genetic polymorphism; types include: albumin b (slow), found occasionally in persons of European ancestry; albumin Ghent (fast), found first at Ghent, Belgium; albumin Mexico (slow), found in Indians of Mexico and the southwestern United States; albumin Naskapi (fast), found in the Naskapi and other Indians of northern North America; and albumin Reading (fast), found first at Reading, England. (05 Mar 2000) |
| albumin tannate | An astringent powder obtained by the action of tannic acid on albumin; contains about 50% tannic acid; used as an astringent disinfectant in diarrhoea and as a dusting powder. (05 Mar 2000) |
| Bence Jones albumin | Proteins with unusual thermosolubility found in the urine of patients with multiple myeloma, consisting of monoclonal immunoglobulin light chains. See: Bence Jones reaction. See: immunoglobulin. (05 Mar 2000) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|