catalog number :
MBS142659
products type :
Native Protein
products full name :
Human Octreotide
products short name :
Octreotide
products name syn :
OCT Human; Octreotide Human
other names :
ornithine carbamoyltransferase, mitochondrial; Ornithine carbamoyltransferase, mitochondrial; ornithine carbamoyltransferase, mitochondrial; OTCase; ornithine transcarbamylase; ornithine carbamoyltransferase; Ornithine transcarbamylase; OTCase
other gene names :
OTC; OTC; OCTD; OTCase
uniprot entry name :
OTC_HUMAN
sequence :
H-D-Phe-Cys-Phe-D-Trp-Lys-Thr-Cys-L-threoninol.
purity :
Greater than 98.0% as determined by RP-HPLC.
form :
The Octreotide was lyophilized from a concentrated (1 mg/ml) solution with no additives. Sterile Filtered White lyophilized (freeze-dried) powder.
storage stability :
Lyophilized Octreotide although stable at room temperature for 3 weeks, should be stored desiccated below -18 degree C. Upon reconstitution Octreotide should be stored at 4 degree C between 2-7 days and for future use below -18 degree C.For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Please prevent freeze-thaw cycles.
other info2 :
Solubility: It is recommended to reconstitute the lyophilized Octreotide in sterile 18M Omega -cm H2O not less than 100 ug/ml, which can then be further diluted to other aqueous solutions.
products categories :
HORMONES; Hormones; Peptide Hormones
products description :
Description: Octreotide Human Synthetic is a single, non-glycosylated, polypeptide chain containing 8 amino acids, having a molecular mass of 1019.26 Dalton and a molecular formula of C49H66N10O10S2.Octreotide is purified by proprietary chromatographic techniques. Introduction: Octreotide acetate is a longer acting synthetic octapeptide analog of naturally occurring somatostatin. It inhibits the secretion of gastro-entero-pancreatic peptide hormones and the release of growth hormone.
ncbi acc num :
NP_000522.3
ncbi gb acc num :
NM_000531.5
ncbi mol weight :
39,935 Da
ncbi pathways :
Arginine And Proline Metabolism Pathway 82957!!Arginine And Proline Metabolism Pathway 323!!Biosynthesis Of Amino Acids Pathway 790012!!Biosynthesis Of Amino Acids Pathway 795174!!Metabolic Pathways 132956!!Metabolism Pathway 477135!!Metabolism Of Amino Acids And Derivatives Pathway 106169!!Urea Cycle Pathway 413351!!Urea Cycle Pathway 106171!!Urea Cycle Pathway 468222
ncbi summary :
This nuclear gene encodes a mitochondrial matrix enzyme. Missense, nonsense, and frameshift mutations in this enzyme lead to ornithine transcarbamylase deficiency, which causes hyperammonemia. Since the gene for this enzyme maps close to that for Duchenne muscular dystrophy, it may play a role in that disease also. [provided by RefSeq, Jul 2008]