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Porcine

The catalytic subunit then catalyzes the direct transfer of the 7-phosphate of ATP (visible as small beads at the end of ATP) to its peptide substrate. Catalysis takes place in the cleft between the two domains. Mutual orientation and position of these two lobes can be classified as either closed or open, for a review of the structures and function see e.g. [36]. The presented structure shows a closed conformation. Both the apoenzyme and the binary complex of the porcine C-subunit with di-iodinated inhibitor peptide represent the crystal structure in an open conformation [37] resulting from an overall rotation of the small lobe relative to the large lobe. [Pg.190]

Biosynthetic Human Insulin from E. coli. Insulin [9004-10-8] a polypeptide hormone, stimulates anaboHc reactions for carbohydrates, proteins, and fats thereby producing a lowered blood glucose level. Porcine insulin [12584-58-6] and bovine insulin [11070-73-8] were used to treat diabetes prior to the availabiHty of human insulin [11061 -68-0]. AH three insulins are similar in amino acid sequence. EH LiHy s human insulin was approved for testing in humans in 1980 by the U.S. EDA and was placed on the market by 1982 (11,12). [Pg.42]

Table 2. Effects of Porcine Somatotropin (pST) Dose on Growth Performance ... Table 2. Effects of Porcine Somatotropin (pST) Dose on Growth Performance ...
U.S.A., in lactating dairy cattie to increase milk production. EH Lilly and Company, The Upjohn Company, and American Cyanamid Company also have interests in the commercial appHcation of recombinant bovine GH. Recombinant porcine GH [9061-23-8] preparations from several companies, eg. The Upjohn Company, Smith Kline Beecham Animal Health, Pitman-Moore, Inc., Monsanto Company, and American Cyanamid Company, are being evaluated for commercial use. Recombinant human GH for clinical use is marketed under such names as Protropin (Genentech), Umatrope (EH Lilly), Genotropin (Sumitomo), and Somatonorm (Kabi-Vitmm) by a variety of pharmaceutical companies. A listing of additional suppHers is available (2). [Pg.176]

Biosynthesis. Somatostatin exists in longer forms in several biological tissues (95,96). One of the longer forms, which has been isolated from porcine intestine, has been characterized as a 28-amino acid peptide (97). Somatostatin is derived from a precursor containing 116 amino acids (98,99). The precursor contains one copy of the somatostatin tetradecapeptide, which is contained within the sequence of the 28-amino acid peptide at the carboxy-terminal end of the precursor. The 28-amino acid somatostatin is preceded by a single Arg residue, while somatostatin 1-14 is preceded by a pair of basic residues. [Pg.203]

NPH Isophane Human Insulin Suspension. NPH isophane insulin, also called Humulin N, Insulatard NPH Human, or Novolin N is an intermediate-acting form of human insulin produced by recombinant DNA techniques. Mixtures Humulin 70/30 and Novolin 70/30 contain 70% NPH isophane and 30% regular, whereas Humulin 50/50 contains 50% NPH isophane and 50% regular. It is adrninistered subcutaneously and should not be given intravenously. Absorption is delayed because the insulin is conjugated with protamine in a complex of reduced isoelectric solubiUty. Therapeutically, this preparation is probably comparable to purified porcine NPH insulin. However, human NPH insulin may have a slightly shorter duration of action than comparable purified porcine products. [Pg.340]

J. Marknssen, Human Insulin by Tryptic Transpeptidation of Porcine Insulin andBiosynthetic Precursors, MTP Press, Lancaster, U.K., 1987. [Pg.343]

Valve Problems. The primary solution to valve problems has been implantable replacement valves. The introduction of these devices necessitates open-heart surgery. There are two types of valves available tissue (porcine and bovine) and mechanical. The disadvantage of tissue valves is that these have a limited life of about seven years before they calcify, stiffen, and have to be replaced. The mechanical valves can last a lifetime, but require anticoagulant therapy. In some patients, anticoagulants may not be feasible or may be contraindicated. Of the valves which require replacement, 99% are mitral and aortic valves. The valves on the left side of the heart are under much greater pressure because the left ventricle is pumping blood out to the entire body, instead of only to the lungs. Occasionally, two valves are replaced in the same procedure. [Pg.181]

Eig. 6. Amino acid sequence of human (H) and porcine (P) calcitonins. [Pg.53]

Hydroxyriboflavin. This compound [86120-61 -8] (26) was isolated as a green coen2yme of the NADH dehydrogenase from Peptostreptococms elsdenii and also from glycolate oxidase of porcine Hver. It is not fluorescent, and its stmcture was estabflshed by synthesis (106). The 5 -monophosphate serves as a cofactor for glycolate oxidase from pig Hver. [Pg.81]


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See also in sourсe #XX -- [ Pg.346 , Pg.353 ]

See also in sourсe #XX -- [ Pg.231 ]

See also in sourсe #XX -- [ Pg.42 ]




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0-Endorphin porcine

Adrenocorticotropic hormone porcine

Brain, porcine

Buccal mucosa porcine permeability

Carboxypeptidase porcine

Collagen porcine shields

Decomposed porcine remains with partial

Enzymatic conversion of porcine insulin

Enzyme catalyzed reaction Porcine pancreatic lipase

Enzymes porcine pancreatic lipase

Esterases porcine liver

Gastric mucosa: human porcine

Growth hormone porcine, effect

Immobilized porcine pancreas lipase

Immobilized porcine pancreas lipase IPPL)

Infectious porcine encephalomyelitis

Insulin porcine, structure

Islet porcine

Isolated perfused porcine skin flap

Isolated perfused porcine skin flap IPPSF)

Isolated perfused porcine skin flap model

Lipase porcine

Mucins porcine stomach

Mucins porcine submaxillary mucin

Mucins submaxillary, porcine

Pepsin porcine

Perfused Porcine Skin Flap

Porcin. pancreatic lipase

Porcine FSH

Porcine LH

Porcine activity

Porcine acylation

Porcine aminopeptidase

Porcine anterior pituitary

Porcine aorta

Porcine brain capillary endothelial cells

Porcine brain microvascular endothelial cells

Porcine brain microvessel endothelial cells

Porcine buccal mucosa

Porcine characterization

Porcine chondrocytes

Porcine classification

Porcine dermis

Porcine elastase

Porcine endogenous retroviruses

Porcine glucagon

Porcine heart

Porcine hver esterase

Porcine insulin

Porcine insulin absorption

Porcine insulin enzymatic conversion

Porcine insulin immunogenicity

Porcine insulin lipoatrophy

Porcine intestinal mucosa

Porcine kidney D-amino acid oxidase

Porcine kidney trehalase

Porcine liver

Porcine liver esterase

Porcine liver molecular weight

Porcine malignant hyperthermia

Porcine microvascular endothelial cell

Porcine monocomponent insulin

Porcine motilin

Porcine myofibrillar protein

Porcine myofibrillar protein hydrolysates

Porcine pancreas

Porcine pancreas lipase

Porcine pancreatic a-amylase

Porcine pancreatic elastase

Porcine pancreatic lipase

Porcine pancreatic lipase asymmetric hydrolysis

Porcine pancreatic lipase, resolution

Porcine pancreatic lipase, resolution esters

Porcine pancreatic polypeptide

Porcine pancreatic trypsin

Porcine parakeratosis

Porcine parvovirus

Porcine pepsin zymogen

Porcine pericardium

Porcine pituitary hormone

Porcine plasma protein

Porcine proinsulin

Porcine pseudorabies virus

Porcine sepsis model

Porcine sequences

Porcine skin

Porcine skin flap model

Porcine somatotropin

Porcine spleen

Porcine stress syndrome

Recombinant porcine somatotropin

Secretin porcine

Sequence porcine pepsin

Stomach porcine

Structure of porcine pancreatic

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