Artikel-Nr:
(BOSSBS-7116R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-7116R-FITC
Lokale Artikelnummer::
BOSSBS-7116R-FITC
Beschreibung:
Ro autoantigens are of clinical significance because directed against them are found in most patients with primary Sjqgren syndrome, subacute cutaneous lupus erythematosus (SLE), neonatal lupus erythematosus, ANA-negative lupus erythematosus, and systemic lupus erythematosus-like disease secondary to homozygous C2 or C4 complement deficiency (1). Ro/SSA is a ribonucleoprotein that binds to auto in 35 to 50% of patients with SLE and in up to 97% of patients with Sjqgren syndrome (2). The Ro/SSA particle consists of a single immunoreactive protein noncovalently bound with one of four small RNA molecules (2). Most anti-Ro/SSA-positive sera detect not only the main protein, but also a smaller Ro/SSA protein (2). The genes which encode the smaller and larger proteins map to human chromosomes 11p15.5 and 1q31, respectively (3?). La/SSB is an autoimmune RNA-binding protein that plays a role in the transcription of RNA polymerase III was originally defined by its reactivity with auto from patients with Sjé°ƒren syndrome and SLE (6).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13627R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R-A647
Lokale Artikelnummer::
BOSSBS-13627R-A647
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13627R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R-A350
Lokale Artikelnummer::
BOSSBS-13627R-A350
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13627R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13627R-HRP
Lokale Artikelnummer::
BOSSBS-13627R-HRP
Beschreibung:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
VE:
1 * 100 µl
Artikel-Nr:
(BIOT004858-0005)
Lieferant:
BIONET RESEARCH
Hersteller-Artikelnummer::
004858-0005
Lokale Artikelnummer::
BIOT004858-0005
Beschreibung:
Lutetiumtrifluorid
VE:
1 * 5 g
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Lieferant:
VWR Chemicals
Beschreibung:
EDTA Dinatriumsalz Dihydrat Ph. Eur., USP, BP, JP, ACS
Artikel-Nr:
(HONE01727.9025)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
01727.9025
Lokale Artikelnummer::
HONE01727.9025
Beschreibung:
Kaliumhexafluorotitanat
VE:
1 * 25 kg
Lieferant:
Avantor
Beschreibung:
EDTA Dinatriumsalz Dihydrat, BAKER, Laborreagens, J.T.Baker®
Artikel-Nr:
(PRSI25-264)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
25-264
Lokale Artikelnummer::
PRSI25-264
Beschreibung:
Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. KCNG1 is a member of the potassium channel, voltage-gated, subfamily G. Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This gene is abundantly expressed in skeletal muscle. Alternative splicing results in at least two transcript variants encoding distinct isoforms. Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This gene is abundantly expressed in skeletal muscle. Multiple alternatively spliced transcript variants have been found in normal and cancerous tissues.
VE:
1 * 50 µG
Lieferant:
Sigma-Aldrich
Beschreibung:
Neodymtrichlorid, Sigma-Aldrich®
Artikel-Nr:
(SIAL483265-100G)
Lieferant:
Sigma-Aldrich
Hersteller-Artikelnummer::
483265-100G
Lokale Artikelnummer::
SIAL483265-100G
Beschreibung:
Antimontriacetat, Sigma-Aldrich®
VE:
1 * 100 g
Lieferant:
Alfa Aesar
Beschreibung:
A synthetic intermediate and a cell-permeable autophagic sequestration blocker that protects cerebellar granule cells from apoptosis post serum/potassium deprivation.
Artikel-Nr:
(REGEEFS3AC)
Lieferant:
REAGECON
Hersteller-Artikelnummer::
EFS3AC
Lokale Artikelnummer::
REGEEFS3AC
Beschreibung:
Kaliumchlorid gesättigt mit Silberchlorid in wäßriger Lösung 3 mol/l (3 N) in wässriger Lösung für die Befüllung von Elektroden
VE:
1 * 100 mL
Artikel-Nr:
(PRSI25-173)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
25-173
Lokale Artikelnummer::
PRSI25-173
Beschreibung:
Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog (s). This gene encodes a member of the potassium channel, voltage-gated, shab-related subfamily. This member is a delayed rectifier potassium channel and its activity is modulated by some other family members.Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. Four sequence-related potassium channel genes - shaker, shaw, shab, and shal - have been identified in Drosophila, and each has been shown to have human homolog (s). This gene encodes a member of the potassium channel, voltage-gated, shab-related subfamily. This member is a delayed rectifier potassium channel and its activity is modulated by some other family members. 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
Lieferant:
Sigma-Aldrich
Beschreibung:
Praseodymtrichlorid Hydrat, Sigma-Aldrich®
Artikel-Nr:
(HONCE2168-100ML)
Lieferant:
Honeywell Chemicals
Hersteller-Artikelnummer::
E2168-100ML
Lokale Artikelnummer::
HONCE2168-100ML
Beschreibung:
Certified Reference Material (CRM).
VE:
1 * 100 mL
Preis auf Anfrage
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