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Wyszukano: Magnesium+tetraborate


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Producent: Thermo Fisher Scientific
Opis: tetraboran dipotasowy tetrahydrat ≥99%
Numer katalogowy: (4503-01)
Producent: Avantor
Opis: tetraboran dilitu, BAKER INSTRA-ANALYZED® for trace metal analysis, J.T.Baker®
j.m.: 1 * 500 g


Producent: Avantor
Opis: tetraboran disodu dekahydrat 99.0-105.0% NF, J.T.Baker®
Producent: VWR Chemicals
Opis: tetraboran disodu dekahydrat 99.0-103.0%, AnalaR NORMAPUR® Reag. Ph. Eur. analytical reagent
Numer katalogowy: (3575-07)
Producent: Avantor
Opis: tetraboran disodu dekahydrat ≥99% NF, Multi-Compendial, J.T.Baker®
j.m.: 1 * 12 kg

MSDS Certyfikaty


Producent: Thermo Fisher Scientific
Opis: tetraboran disodu, anhydrous ≥99.998% (metals basis), Puratronic®
Numer katalogowy: (PRSI6289)
Producent: ProSci Inc.
Opis: ATP2C2 Antibody: ATP2C2, also known as secretory pathway Ca2+/Mn2+-ATPase (SPCA) 2, belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium from the cytosol to the Golgi lumen. Defects in the related gene ATP2C1 cause Hailey-Hailey disease, for which ATP2C2 does not compensate, suggesting that ATP2C2 plays other physiological roles. Unlike ATP2C1, ATP2C2 has a much more restricted expression pattern and displays a higher maximal turnover rate for overall Ca2+-ATPase reaction and a lower apparent affinity for cytosolic Ca2+ activation of phosphorylation. Overexpression of ATP2C2 in mammary tumors result a Ca2+ influx via the store-operated Ca2+ channel ORAI1 and independent of the STIM1 and STIM2 sensors.
j.m.: 1 * 100 µG


Producent: Thermo Fisher Scientific
Opis: tetraboran dilitu ≥99.6% (metals basis)
Numer katalogowy: (BOSSBS-13132R-A680)
Producent: Bioss
Opis: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
j.m.: 1 * 100 µl


Numer katalogowy: (7418-26)
Producent: MACRON AVANTOR BRAND
Opis: tetraboran disodu dekahydrat 99.0-105.0% NF, Macron Fine Chemicals™
j.m.: 1 * 300 lb

MSDS Certyfikaty


Numer katalogowy: (27721.366)
Producent: VWR Chemicals
Opis: tetraboran disodu dekahydrat ≥98%, purified
j.m.: 1 * 5 kg

MSDS Certyfikaty


Producent: Thermo Fisher Scientific
Opis: tetraboran disodu, anhydrous ≥99.95% (metals basis)
Numer katalogowy: (BOSSBS-13132R-A488)
Producent: Bioss
Opis: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
j.m.: 1 * 100 µl


Numer katalogowy: (BOSSBS-13132R-FITC)
Producent: Bioss
Opis: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
j.m.: 1 * 100 µl


Producent: MACRON AVANTOR BRAND
Opis: tetraboran disodu dekahydrat 99.5-105.0%, granular, AR® ACS, Macron Fine Chemicals™
Numer katalogowy: (7792-88)
Producent: MACRON AVANTOR BRAND
Opis: tetraboran disodu dekahydrat 99.0-105.0%, GenAR® NF for biotechnology, Macron Fine Chemicals™
j.m.: 1 * 12 kg

MSDS Certyfikaty


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Zapasy tego artykułu są ograniczone, ale możliwe, że jest on dostępny w pobliskim magazynie. Upewnij się, że jesteś zalogowany na stronie, aby móc sprawdzić dostępność zapasów. Jeśli call ciągle się wyświetla i potrzebujesz pomocy, zadzwoń na 58 323 82 00.
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