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Methyl-(R)-(+)-lactat
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Methyl-(R)-(+)-lactat
Artikel-Nr:
(BOSSBS-8071R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8071R-A350
Lokale Artikelnummer::
BOSSBS-8071R-A350
Beschreibung:
May be a chaperone-like protein essential for the proper conformation and functioning of protein complexes in the respiratory chain.Tissue specificity:Ubiquitously expressed with a relatively greater abundance in heart and skeletal muscle.Involvement in disease:Defects in ADCK3 are a cause of coenzyme Q10 deficiency (CoQ10 deficiency). CoQ10 deficiency is an autosomal recessive disorder with variable manifestations. It can be associated with three main clinical phenotypes: a predominantly myopathic form with central nervous system involvement, an infantile encephalomyopathy with renal dysfunction and an ataxic form with cerebellar atrophy.Defects in ADCK3 are the cause of spinocerebellar ataxia autosomal recessive type 9 (SCAR9) [MIM:612016]; also known as autosomal recessive cerebellar ataxia type 2 (ARCA2). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR9 is an autosomal recessive form characterized by gait ataxia and cerebellar atrophy with slow progression and few associated features. Patients can manifest brisk tendon reflexes and Hoffmann sign, mild psychomotor retardation, mild axonal degeneration of the sural nerve, exercise intolerance and elevated serum lactate.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8071R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8071R-A647
Lokale Artikelnummer::
BOSSBS-8071R-A647
Beschreibung:
May be a chaperone-like protein essential for the proper conformation and functioning of protein complexes in the respiratory chain.Tissue specificity:Ubiquitously expressed with a relatively greater abundance in heart and skeletal muscle.Involvement in disease:Defects in ADCK3 are a cause of coenzyme Q10 deficiency (CoQ10 deficiency). CoQ10 deficiency is an autosomal recessive disorder with variable manifestations. It can be associated with three main clinical phenotypes: a predominantly myopathic form with central nervous system involvement, an infantile encephalomyopathy with renal dysfunction and an ataxic form with cerebellar atrophy.Defects in ADCK3 are the cause of spinocerebellar ataxia autosomal recessive type 9 (SCAR9) [MIM:612016]; also known as autosomal recessive cerebellar ataxia type 2 (ARCA2). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR9 is an autosomal recessive form characterized by gait ataxia and cerebellar atrophy with slow progression and few associated features. Patients can manifest brisk tendon reflexes and Hoffmann sign, mild psychomotor retardation, mild axonal degeneration of the sural nerve, exercise intolerance and elevated serum lactate.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Bovine L-Lactate dehydrogenase Typ XVII (from Heart)
Lieferant:
Serva
Beschreibung:
L-Lactat-Dehydrogenase (vom Muskel)
Artikel-Nr:
(FITZ20-LG22)
Lieferant:
Fitzgerald Industries
Hersteller-Artikelnummer::
20-LG22
Lokale Artikelnummer::
FITZ20-LG22
Beschreibung:
L-Lactat-Dehydrogenase
VE:
1 * 1 mL
Lieferant:
Sigma-Aldrich
Beschreibung:
L-Lactat-Dehydrogenase Typ II (vom Muskel)
Lieferant:
Sigma-Aldrich
Beschreibung:
L-Lactat-Dehydrogenase Typ XI (vom Muskel)
Artikel-Nr:
(ABCAAB134187-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB134187-100
Lokale Artikelnummer::
ABCAAB134187-100
Beschreibung:
Anti-Lactate Dehydrogenase Rabbit Monoclonal Antibody [clone: EP1563Y]
VE:
1 * 100 µl
 This is a MarketSource item. Additional charges may apply
Artikel-Nr:
(HONCE3023-100ML)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
E3023-100ML
Lokale Artikelnummer::
HONCE3023-100ML
Beschreibung:
Certified Reference Material (CRM)
VE:
1 * 100 mL
Lieferant:
Spectrum Chemical
Beschreibung:
Sodium DL-Lactate Solution, 60 Percent (w/w), USP is used for the restoration of extracellular fluid and electrolytes balances. All Spectrum Chemical USP products are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.
Artikel-Nr:
(ABCAAB53292-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB53292-100
Lokale Artikelnummer::
ABCAAB53292-100
Beschreibung:
Anti-Lactate Dehydrogenase Rabbit Monoclonal Antibody [clone: EP1565Y]
VE:
1 * 100 µl
This is a MarketSource item. Additional charges may apply
Lieferant:
ACTIVE MOTIF
Beschreibung:
Lactat-Standardlösung, 1000 mg/l, Matrix: H₂O, Anwendung: Ionenchromatographie-Standards
Lieferant:
MP Biomedicals
Beschreibung:
Lactic acid is an α hydroxyl carboxylic acid produced from pyruvate by the enzyme lactate dehydrogenase (LDH). Lactate is one of the main components of Ringer′s lactate or lactated Ringer′s solution. It is a fermentation acid from milk or carbohydrates.
Artikel-Nr:
(BOSSBS-8071R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8071R-A750
Lokale Artikelnummer::
BOSSBS-8071R-A750
Beschreibung:
May be a chaperone-like protein essential for the proper conformation and functioning of protein complexes in the respiratory chain.Tissue specificity:Ubiquitously expressed with a relatively greater abundance in heart and skeletal muscle.Involvement in disease:Defects in ADCK3 are a cause of coenzyme Q10 deficiency (CoQ10 deficiency). CoQ10 deficiency is an autosomal recessive disorder with variable manifestations. It can be associated with three main clinical phenotypes: a predominantly myopathic form with central nervous system involvement, an infantile encephalomyopathy with renal dysfunction and an ataxic form with cerebellar atrophy.Defects in ADCK3 are the cause of spinocerebellar ataxia autosomal recessive type 9 (SCAR9) [MIM:612016]; also known as autosomal recessive cerebellar ataxia type 2 (ARCA2). Spinocerebellar ataxia is a clinically and genetically heterogeneous group of cerebellar disorders. Patients show progressive incoordination of gait and often poor coordination of hands, speech and eye movements, due to degeneration of the cerebellum with variable involvement of the brainstem and spinal cord. SCAR9 is an autosomal recessive form characterised by gait ataxia and cerebellar atrophy with slow progression and few associated features. Patients can manifest brisk tendon reflexes and Hoffmann sign, mild psychomotor retardation, mild axonal degeneration of the sural nerve, exercise intolerance and elevated serum lactate.
VE:
1 * 100 µl
Lieferant:
Spectrum Chemical
Beschreibung:
Calcium Lactate, Pentahydrate, USP, FCC, EP is a filler/diluent excipient.
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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