DL-Ornithin+Hydrochlorid
Lieferant:
Biotium
Beschreibung:
Nitric oxide donors, nitric oxide synthase inhibitors and nitric oxide detection reagents and kits for nitric oxide (NO) studies.
Artikel-Nr:
(PRSI33-424)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
33-424
Lokale Artikelnummer::
PRSI33-424
Beschreibung:
This protein is involved in the pathway that synthesizes L-ornithine and urea from L-arginine.
VE:
1 * 100 µG
New Product
Artikel-Nr:
(BSBTA00721-1)
Lieferant:
BosterBio
Hersteller-Artikelnummer::
A00721-1
Lokale Artikelnummer::
BSBTA00721-1
Beschreibung:
Rabbit IgG polyclonal antibody for Ornithine carbamoyltransferase, mitochondrial(OTC) detection. Tested with WB in Human;Mouse;Rat.
VE:
1 * 100 µG
Artikel-Nr:
(PRSI34-148)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
34-148
Lokale Artikelnummer::
PRSI34-148
Beschreibung:
Recognises a 53 kDa protein, identified as the Ornithine Decarboxylase (ODC-1). ODC is the initial and rate-limiting enzyme in the biosynthetic pathway of polyamines and is involved in the conversion of ornithine to putrescine. The biological activity of ODC-1 is rapidly induced in response to virtually all agents known to promote cell proliferation including hormones, drugs, growth factors, mitogens, and tumor promoters. Reportedly, ODC mRNA levels are elevated in lung carcinomas as well as in colon adenomas and carcinomas. ODC activity in colorectal carcinomas is greater than those in adenomas and normal mucosa.
VE:
1 * 100 µG
New Product
Artikel-Nr:
(PRSI33-451)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
33-451
Lokale Artikelnummer::
PRSI33-451
Beschreibung:
Recognises a 53 kDa protein, identified as the Ornithine Decarboxylase (ODC-1). ODC is the initial and rate-limiting enzyme in the biosynthetic pathway of polyamines and is involved in the conversion of ornithine to putrescine. The biological activity of ODC-1 is rapidly induced in response to virtually all agents known to promote cell proliferation including hormones, drugs, growth factors, mitogens, and tumor promoters. Reportedly, ODC mRNA levels are elevated in lung carcinomas as well as in colon adenomas and carcinomas. ODC activity in colorectal carcinomas is greater than those in adenomas and normal mucosa.
VE:
1 * 100 µG
New Product
Artikel-Nr:
(J60890.MF)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
J60890.MF
Lokale Artikelnummer::
ALFAJ60890.MF
Beschreibung:
Nω-Methyl-L-arginine monoacetate ≥99%
VE:
1 * 50 mg
Artikel-Nr:
(PRSI96-034)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
96-034
Lokale Artikelnummer::
PRSI96-034
Beschreibung:
Arginase-1 (ARG1) is also known as Liver-type arginase, Type I arginase, which belongs to the arginase family. Arginase-1 / ARG1 is a manganese-containing enzyme. The reaction catalysed by this enzyme is: arginine + H2O → ornithine + urea. It is the final enzyme of the urea cycle. Defects in Arginase-1 / ARG1 are the cause of argininemia (ARGIN).
VE:
1 * 50 µG
Artikel-Nr:
(PRSI33-450)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
33-450
Lokale Artikelnummer::
PRSI33-450
Beschreibung:
Recognises a 53 kDa protein, identified as the Ornithine Decarboxylase (ODC-1). ODC is the initial and rate-limiting enzyme in the biosynthetic pathway of polyamines and is involved in the conversion of ornithine to putrescine. The biological activity of ODC-1 is rapidly induced in response to virtually all agents known to promote cell proliferation including hormones, drugs, growth factors, mitogens, and tumor promoters. Reportedly, ODC mRNA levels are elevated in lung carcinomas as well as in colon adenomas and carcinomas. ODC activity in colorectal carcinomas is greater than those in adenomas and normal mucosa.
VE:
1 * 100 µG
New Product
Artikel-Nr:
(PRSI33-951)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
33-951
Lokale Artikelnummer::
PRSI33-951
Beschreibung:
Arginase catalyses the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterised by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [RefSeq].
VE:
1 * 100 µG
New Product
Artikel-Nr:
(PRSI30-093)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
30-093
Lokale Artikelnummer::
PRSI30-093
Beschreibung:
Arginase catalyzes the hydrolysis of arginine to ornithine and urea. The type I isoform of ARG1, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.
VE:
1 * 100 µG
Artikel-Nr:
(PRSI30-092)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
30-092
Lokale Artikelnummer::
PRSI30-092
Beschreibung:
Arginase catalyzes the hydrolysis of arginine to ornithine and urea. The type I isoform of ARG1, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia.
VE:
1 * 100 µG
Artikel-Nr:
(PRSI91-585)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
91-585
Lokale Artikelnummer::
PRSI91-585
Beschreibung:
GFER is a hepatotrophic growth factor and flavin-linked sulfhydryl oxidase which belongs to the Erv1/ALR family of proteins. GFER is widely expressed in various human tissues. They are two isoforms of this protein. Isoform 1 could regenerate the redox-active disulfide bonds in CHCHD4/MIA40, a chaperone essential for disulfide bond formation and protein folding in the mitochondrial intermembrane space. The reduced form of CHCHD4/MIA40 forms a transient intermolecular disulfide bridge with GFER/ERV1, resulting in regeneration of the essential disulfide bonds in CHCHD4/MIA40, while GFER/ERV1 becomes re-oxidized by donating electrons to cytochrome c or molecular oxygen. Isoform 2 may act as an autocrine hepatotrophic growth factor promoting liver regeneration. GFER could also induce the expression of S-adenosylmethionine decarboxyl-ase and ornithine decarboxylases (ODC). S-adenosylmethionine decarboxyl-ase and ornithine decarboxylases play an important role in the synthesis of polyamines.
VE:
1 * 50 µG
Artikel-Nr:
(PRSI92-205)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
92-205
Lokale Artikelnummer::
PRSI92-205
Beschreibung:
ARG1 is a member of the ureohydrolase family of enzymes. ARG1 can catalyse the hydrolysis of arginine to ornithine and urea. In the urea cycle, ARG1 catalyses the fifth and final step, a series of biochemical reactions in mammals during which the body disposes of harmful ammonia. ARG1 is a cytosolic enzyme and expressed widely in the liver as part of the urea cycle. Inherited deficiency of this ARG1 causes argininemia, which is an autosomal recessive disorder characterised by hyperammonemia.
VE:
1 * 50 µG
Artikel-Nr:
(PRSI25-230)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
25-230
Lokale Artikelnummer::
PRSI25-230
Beschreibung:
CNBP is a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene.This gene encodes a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene.
VE:
1 * 50 µG
Artikel-Nr:
(PRSI25-470)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
25-470
Lokale Artikelnummer::
PRSI25-470
Beschreibung:
ZNF281 belongs to the krueppel C2H2-type zinc-finger protein family. It contains 4 C2H2-type zinc fingers. ZNF281 may be involved in transcriptional regulation. It represses the transcription of a number of genes including gastrin and ornithine decarboxylase. ZNF281 binds to the G-rich box in the enhancer region of these genes.
VE:
1 * 50 µG
Artikel-Nr:
(PRSI26-892)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
26-892
Lokale Artikelnummer::
PRSI26-892
Beschreibung:
Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exists (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. ARG2 (type II isoform) is located in the mitochondria and expressed in extra-hepatic tissues, especially kidney. The physiologic role of this isoform is poorly understood; it is thought to play a role in nitric oxide and polyamine metabolism.Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exists (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type II isoform encoded by this gene, is located in the mitochondria and expressed in extra-hepatic tissues, especially kidney. The physiologic role of this isoform is poorly understood; it is thought to play a role in nitric oxide and polyamine metabolism. Transcript variants of the type II gene resulting from the use of alternative polyadenylation sites have been described. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
VE:
1 * 50 µG
Preis auf Anfrage
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