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L(-)-Glutathion+(oxidierte+Form)
Artikel-Nr:
(BOSSBS-2723R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2723R-A350
Lokale Artikelnummer::
BOSSBS-2723R-A350
Beschreibung:
May have a role in chronic inflammations and may stimulate production of constitutive rather than inflammatory chemokines and cytokines. Forms a receptor signaling complex with TYROBP and triggers activation of the immune responses in macrophages and dendritic cells.
VE:
1 * 100 µl
Artikel-Nr:
(ROCK200-301-400)
Lieferant:
Rockland Immunochemicals
Hersteller-Artikelnummer::
200-301-400
Lokale Artikelnummer::
ROCK200-301-400
Beschreibung:
Protein A Purified Mab anti-ATM has been tested by ELISA and western blotting against both the native and recombinant forms of the Protein. The antibody immunoprecipitates ATM from irradiated human and transfected mouse cells.
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-6671R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6671R-CY5.5
Lokale Artikelnummer::
BOSSBS-6671R-CY5.5
Beschreibung:
Pore-forming (alpha) subunit of voltage-gated rapidly inactivating A-type potassium channels. May contribute to I(To) current in heart and I(Sa) current in neurons. Channel properties are modulated by interactions with other alpha subunits and with regulatory subunits.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-6671R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6671R-A488
Lokale Artikelnummer::
BOSSBS-6671R-A488
Beschreibung:
Pore-forming (alpha) subunit of voltage-gated rapidly inactivating A-type potassium channels. May contribute to I(To) current in heart and I(Sa) current in neurons. Channel properties are modulated by interactions with other alpha subunits and with regulatory subunits.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9452R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9452R-HRP
Lokale Artikelnummer::
BOSSBS-9452R-HRP
Beschreibung:
Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits thereby driving them into their inactive GDP-bound form. Activity on G(z)-alpha is inhibited by phosphorylation of the G-protein. Activity on G(z)-alpha and G(i)-alpha-1 is inhibited by palmitoylation of the G-protein.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-1682R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-1682R-A750
Lokale Artikelnummer::
BOSSBS-1682R-A750
Beschreibung:
CIB1(Calcium and integrin binding 1) may convert the inactive conformation of integrin alpha-IIb/beta3 to an active form through the binding to the integrin cytoplasmic domain.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4562R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4562R-A350
Lokale Artikelnummer::
BOSSBS-4562R-A350
Beschreibung:
Metabolizes several precarcinogens, drugs, and solvents to reactive metabolites. Inactivates a number of drugs and xenobiotics and also bioactivates many xenobiotic substrates to their hepatotoxic or carcinogenic forms.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-0154R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-0154R-A488
Lokale Artikelnummer::
BOSSBS-0154R-A488
Beschreibung:
This protein is associated with nerve growth. It is a major component of the motile "growth cones" that form the tips of elongating axons. Plays a role in axonal and dendritic filopodia induction.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8071R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8071R-HRP
Lokale Artikelnummer::
BOSSBS-8071R-HRP
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-8338R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8338R-A680
Lokale Artikelnummer::
BOSSBS-8338R-A680
Beschreibung:
Defects in PANK2 are the cause of neurodegeneration with brain iron accumulation type 1 (NBIA1); also known as pantothenate kinase-associated neurodegeneration (PKAN) or Hallervorden-Spatz syndrome (HSS). It is an autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain, primarily in the basal ganglia. Clinical manifestations include progressive muscle spasticity, hyperreflexia, muscle rigidity, dystonia, dysarthria, and intellectual deterioration which progresses to severe dementia over several years. It is clinically classified into classic, atypical, and intermediate phenotypes. Classic forms present with onset in the first decade, rapid progression, loss of independent ambulation within 15 years. Atypical forms have onset in the second decade, slow progression, maintenance of independent ambulation up to 40 years later. Intermediate forms manifest onset in the first decade with slow progression or onset in the second decade with rapid progression. Patients with early onset tend to also develop pigmentary retinopathy, whereas those with later onset tend to also have speech disorders and psychiatric features. All patients have the 'eye of the tiger' sign on brain MRI.Defects in PANK2 are the cause of hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP). HARP is a rare syndrome with many clinical similarities to NBIA1.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2794R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2794R-FITC
Lokale Artikelnummer::
BOSSBS-2794R-FITC
Beschreibung:
Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits thereby driving them into their inactive GDP-bound form. Binds to G(i)-alpha and G(o)-alpha, but not to G(s)-alpha.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-2794R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-2794R-A680
Lokale Artikelnummer::
BOSSBS-2794R-A680
Beschreibung:
Inhibits signal transduction by increasing the GTPase activity of G protein alpha subunits thereby driving them into their inactive GDP-bound form. Binds to G(i)-alpha and G(o)-alpha, but not to G(s)-alpha.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4611R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4611R-HRP
Lokale Artikelnummer::
BOSSBS-4611R-HRP
Beschreibung:
Forms a water-specific channel that provides the plasma membranes of renal collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4611R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4611R-A680
Lokale Artikelnummer::
BOSSBS-4611R-A680
Beschreibung:
Forms a water-specific channel that provides the plasma membranes of renal collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4043R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4043R-A680
Lokale Artikelnummer::
BOSSBS-4043R-A680
Beschreibung:
UGP2 (UDP glucose pyrophosphorylase 2) is an important intermediary in cellular metabolic pathways. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP glucose and MgPPi.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4611R-PE)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4611R-PE
Lokale Artikelnummer::
BOSSBS-4611R-PE
Beschreibung:
Forms a water-specific channel that provides the plasma membranes of renal collecting duct with high permeability to water, thereby permitting water to move in the direction of an osmotic gradient.
VE:
1 * 100 µl
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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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