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Hledali jste: Methylene+Green+zinc+chloride+double+salt


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Katalogové číslo: (1.13720.0009)
Dodavatel: Merck
Popis: Dichlormethan-D2 (99.8% D) for NMR spectroscopy, Sigma-Aldrich®
Měrná jednotka: 1 * 7,5 mL

Dodavatel: Merck
Popis: Dichlormethan-D2, Sigma-Aldrich®

Dodavatel: Merck
Popis: Methylenová modř ≥82% (dye content), certified by the Biological Stain Commission, Sigma-Aldrich®

Dodavatel: Thermo Fisher Scientific
Popis: Dichlormethan 99.5% stabilizovaný p.a.
Dodavatel: Merck
Popis: Azomethine H sodium salt, Supelco®
Katalogové číslo: (HEWL5190-0472)
Dodavatel: Agilent
Popis: Standard for GC-MS, GC/MS pesticide analyzer internal standard, phenanthrene-d10 at 1000 µg/ml in methylene: chloride, 4×1 ml
Měrná jednotka: 1 * 1 KS


Katalogové číslo: (48900-U)
Dodavatel: Merck
Popis: EPA TCL Base/Neutrals Mix 1, Supelco®, Certified reference material, 2000 mug/mL each component in methylene chloride, : N/A
Měrná jednotka: 1 * 1 KS


Dodavatel: Thermo Fisher Scientific
Popis: Dichlormethan 99.8% stabilised for HPLC
Dodavatel: Apollo Scientific
Popis: Chlorid sodný pure USP, BP, Ph. Eur., JP, pharma grade

Katalogové číslo: (BOSSBS-7344R-A350)
Dodavatel: Bioss
Popis: The 2'- 5'- oligoadenylate synthetase (OAS) family is comprised of four members: OAS1, OAS2, OAS3 and OASL. These proteins are induced by interferons and function to convert ATP into 2'- 5'- linked oligomers of adenosine in the presence of double-stranded RNA and magnesium ions. Copper, iron and zinc ions strongly inhibit the OAS enzymatic activity, while manganese ions can replace magnesium ions as an activator. The OAS family plays a significant role in the inhibition of cellular protein synthesis, apoptosis and growth, and its members are important factors in viral infection resistance. OAS3, also referred to as p100, contains three adjacent OAS1-like domains and maps to the human chromosome 12q24.2
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-7344R-A647)
Dodavatel: Bioss
Popis: The 2'- 5'- oligoadenylate synthetase (OAS) family is comprised of four members: OAS1, OAS2, OAS3 and OASL. These proteins are induced by interferons and function to convert ATP into 2'- 5'- linked oligomers of adenosine in the presence of double-stranded RNA and magnesium ions. Copper, iron and zinc ions strongly inhibit the OAS enzymatic activity, while manganese ions can replace magnesium ions as an activator. The OAS family plays a significant role in the inhibition of cellular protein synthesis, apoptosis and growth, and its members are important factors in viral infection resistance. OAS3, also referred to as p100, contains three adjacent OAS1-like domains and maps to the human chromosome 12q24.2
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-7344R-A750)
Dodavatel: Bioss
Popis: The 2'- 5'- oligoadenylate synthetase (OAS) family is comprised of four members: OAS1, OAS2, OAS3 and OASL. These proteins are induced by interferons and function to convert ATP into 2'- 5'- linked oligomers of adenosine in the presence of double-stranded RNA and magnesium ions. Copper, iron and zinc ions strongly inhibit the OAS enzymatic activity, while manganese ions can replace magnesium ions as an activator. The OAS family plays a significant role in the inhibition of cellular protein synthesis, apoptosis and growth, and its members are important factors in viral infection resistance. OAS3, also referred to as p100, contains three adjacent OAS1-like domains and maps to the human chromosome 12q24.2
Měrná jednotka: 1 * 100 µl


Dodavatel: Thermo Fisher Scientific
Popis: Dichlormethan 99.6% stabilizovaný ACS
Katalogové číslo: (BOSSBS-12442R-A488)
Dodavatel: Bioss
Popis: The ABLIM1 protein has an N-terminal domain that contains four double zinc finger motifs, which conform to the LIM motif consensus sequence. ABLIM1 binds to F-Actin through a dematin-like domain and is expressed in retina, brain and muscle tissue. There are four known isoforms of ABLIM1. The gene encoding ABLIM1 maps to a region of chromosome 10 associated with frequent loss of heterozygosity in human tumors, thus identifying ABLIM1 as a candidate tumor suppressor gene. ABLIM2 and ABLIM3 show highest expression in muscle and neuronal tissues, bind to F-Actin, and are localized on stress fibers. They also have been shown to enhance STARS (striated muscle activator of Rho signaling) dependent activation of serum-response factor (SRF), thereby modulating transcription.
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-12489R-CY3)
Dodavatel: Bioss
Popis: APLF is a 511 amino acid protein that contains one FHA doman and two C2H2type zinc fingers. Localized to both the nucleus and the cytoplasm, APLF interacts with XRCC1, XRCC4 and Ku-86 and, via these interactions, is involved in single-strand and double-strand DNA break repair. APLF is subject to post-translational phosphorylation in response to DNA breaks. The gene encoding APLF maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-12489R-CY5)
Dodavatel: Bioss
Popis: APLF is a 511 amino acid protein that contains one FHA doman and two C2H2type zinc fingers. Localized to both the nucleus and the cytoplasm, APLF interacts with XRCC1, XRCC4 and Ku-86 and, via these interactions, is involved in single-strand and double-strand DNA break repair. APLF is subject to post-translational phosphorylation in response to DNA breaks. The gene encoding APLF maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
Měrná jednotka: 1 * 100 µl


Cena na vyžádání
Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
Omezené množství produktu na skladě. Zboží může být k dispozici v jiném skladě poblíž vašeho sídla. Přesvědčte se, že jste přihlášení na stránky, abyste mohli vidět dostupné položky na skladě. Pokud je stále zobrazeno call a potřebujete asistenci, volejte na číslo 321 570 321.
Daná chemikálie je regulována dle platné legislativy a bude vyžadováno vyplnění formuláře. Jeho včasným vyplněním uspíšíte dodání produktu.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
Tento produkt je zablokován vaší organizací. Kontaktujte své nákupní oddělení pro více informací.
Původní produkt již není k dispozici. Zobrazen je náhradní produkt.
Tento produkt již není k dispozici. Podobné produkty můžete vyhledat pomocí VWR katalogových čísel nebo čísel dodavatele uvedených výše. Pokud potřebujete další asistenci, zavolejte na telefonní číslo zákaznického servisu VWR 321 570 321.
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