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Image Unavailable-50002.

BAPTA tetrapotassium salt ≥95% (durch TLC) Ionen-Chelator, zur Kalziumbestimmung

Artikel-Nr: (50002.)
Lieferant: Biotium
Beschreibung: BAPTA and its derivatives are calcium chelators that are commonly used to form calcium buffers with well-defined calcium concentrations. By injecting the chelators into cells or by incubating cells with the AM ester form of the chelators, one can control the cytosolic calcium concentration, an important means to study the roles of calcium. Key advantages of these calcium chelators include relative insensitivity toward intracellular pH change and fast release of calcium.
VE: 1 * 1 g
Image Unavailable-50006.

5,5'-difluoro BAPTA tetrapotassium salt ≥95% (durch TLC) Ionen-Chelator, zur Kalziumbestimmung

Artikel-Nr: (50006.)
Lieferant: Biotium
Beschreibung: BAPTA and its derivatives are calcium chelators that are commonly used to form calcium buffers with well-defined calcium concentrations. By injecting the chelators into cells or by incubating cells with the AM ester form of the chelators, one can control the cytosolic calcium concentration, an important means to study the roles of calcium.
VE: 1 * 100 mg
Image Unavailable-BOSSBS-8228R

Anti-FAHD2A Rabbit Polyclonal Antibody

Artikel-Nr: (BOSSBS-8228R)
Lieferant: Bioss
Beschreibung: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-8228R-CY5

Anti-FAHD2A Rabbit Polyclonal Antibody (Cy5®)

Artikel-Nr: (BOSSBS-8228R-CY5)
Lieferant: Bioss
Beschreibung: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
VE: 1 * 100 µl
Image Unavailable-50041.

Indo-1 pentapotassium salt ≥90% (durch HPLC) fluoreszierender Indikator, zur Kalziumbestimmung

Artikel-Nr: (50041.)
Lieferant: Biotium
Beschreibung: Membrane-impermeant calcium indicator that can be loaded into cells via microinjection or scrape loading.
VE: 1 * 1 mg
Image Unavailable-50040.

Indo-1 pentammonium salt ≥95% (durch TLC) fluoreszierender Indikator, zur Kalziumbestimmung

Artikel-Nr: (50040.)
Lieferant: Biotium
Beschreibung: Membrane-impermeant calcium indicator that can be loaded into cells via microinjection or scrape loading.
VE: 1 * 1 mg
Image Unavailable-50003.

BAPTA tetrasodium salt ≥95% (durch TLC) Ionen-Chelator, zur Kalziumbestimmung

Artikel-Nr: (50003.)
Lieferant: Biotium
Beschreibung: BAPTA and its derivatives are calcium chelators that are commonly used to form calcium buffers with well-defined calcium concentrations. By injecting the chelators into cells or by incubating cells with the AM ester form of the chelators, one can control the cytosolic calcium concentration, an important means to study the roles of calcium.
VE: 1 * 1 g
Image Unavailable-50030.

FURA-2 pentaammonium salt ≥95% (durch HPLC) fluoreszierender Indikator, zur Kalziumbestimmung

Artikel-Nr: (50030.)
Lieferant: Biotium
Beschreibung: Fura-2, pentaammonium salt is a ratiometric fluorescent dye that binds to free intracellular calcium. It is membrane-impermeant and may be loaded into cells via microinjection or scrape loading.
VE: 1 * 1 mg
Image Unavailable-BOSSBS-8228R-A750

Anti-FAHD2A Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Artikel-Nr: (BOSSBS-8228R-A750)
Lieferant: Bioss
Beschreibung: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilise calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is also associated with mutations to chromosome 2.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-8228R-A647

Anti-FAHD2A Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Artikel-Nr: (BOSSBS-8228R-A647)
Lieferant: Bioss
Beschreibung: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-8228R-CY3

Anti-FAHD2A Rabbit Polyclonal Antibody (Cy3®)

Artikel-Nr: (BOSSBS-8228R-CY3)
Lieferant: Bioss
Beschreibung: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
VE: 1 * 100 µl
Image Unavailable-BOSSBS-8228R-A350

Anti-FAHD2A Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Artikel-Nr: (BOSSBS-8228R-A350)
Lieferant: Bioss
Beschreibung: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
VE: 1 * 100 µl
Image Unavailable-L08214.06

DL-Glycerinsäure Hemicalciumsalz-Hydrat

Lieferant: Thermo Fisher Scientific
Beschreibung: DL-Glycerinsäure Hemicalciumsalz-Hydrat

Sicherheitsdatenblätter Zertifikate

Image Unavailable-50032.

FURA-2 pentasodium salt ≥95% (durch HPLC) fluoreszierender Indikator, zur Kalziumbestimmung

Artikel-Nr: (50032.)
Lieferant: Biotium
Beschreibung: Fura-2, pentasodium salt is a ratiometric fluorescent dye that binds to free intracellular calcium. It is membrane-impermeant and may be loaded into cells via microinjection or scrape loading.
VE: 1 * 1 mg
Image Unavailable-50004.

5,5′-Dibromo BAPTA tetrapotassium salt ≥95% (durch TLC) Ionen-Chelator, zur Kalziumbestimmung

Artikel-Nr: (50004.)
Lieferant: Biotium
Beschreibung: BAPTA and its derivatives are calcium chelators that are commonly used to form calcium buffers with well-defined calcium concentrations. By injecting the chelators into cells or by incubating cells with the AM ester form of the chelators, one can control the cytosolic calcium concentration, an important means to study the roles of calcium.
VE: 1 * 100 mg
Image Unavailable-50042.

Indo-1 pentasodium salt ≥95% (durch HPLC) fluoreszierender Indikator, zur Kalziumbestimmung

Artikel-Nr: (50042.)
Lieferant: Biotium
Beschreibung: Membrane-impermeant calcium indicator that can be loaded into cells via microinjection or scrape loading.
VE: 1 * 1 mg
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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 call noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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