Du Søgte efter: Hygromycin+B

Varenummer: (A5347.0100)

Leverandør: PanReac AppliChem

Beskrivelse: Hygromycin B

UOM: 1 * 100 mg

Tilbud

Leverandør: TCI

Beskrivelse: Hygromycin B ≥80.0% (by HPLC)

Varenummer: (APOSBIH4302-1G)

Leverandør: Apollo Scientific

Beskrivelse: Toxic aminoglycoside produced by Streptomyces hygroscopicus. Used as a selective agent for the incorporation of the APH-4 gene in plant tissue.

UOM: 1 * 1 g

Certifikater Tilbud

Varenummer: (APOSBIH0125-20ML)

Leverandør: Apollo Scientific

Beskrivelse: Toxic aminoglycoside produced by Streptomyces hygroscopicus. Used as a selective agent for the incorporation of the APH-4 gene in plant tissue.

UOM: 1 * 20 mL

Tilbud

Varenummer: (ICNA0215751383)

Leverandør: MP Biomedicals

Beskrivelse: Hygromycin B is an aminoglycoside antibiotic produced by the bacterium Streptomyces hygroscopicus that kills bacteria, fungi and higher eukaryotic cells by inhibiting protein synthesis.

UOM: 1 * 1 Each

Tilbud

Leverandør: Roth Carl

Beskrivelse: Hygromycin B 50 mg/ml i vandigopløsning

Varenummer: (BOSSBS-5353R-A680)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anaemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anaemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-5353R-HRP)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-5353R)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-5353R-CY3)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4106R-CY3)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Leverandør: Cayman Chemical

Beskrivelse: Hygromycin B

MSDS Certifikater

Varenummer: (BOSSBS-4106R-CY7)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-5353R-A555)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4106R-HRP)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud

Varenummer: (BOSSBS-4106R-A350)

Leverandør: Bioss

Beskrivelse: FANCG, involved in Fanconi anemia, confers resistance to both hygromycin and mitomycin C. FANCG contains a 5-prime GC-rich untranslated region characteristic of housekeeping genes. The putative 622-amino acid protein has a leucine-zipper motif at its N-terminus. Fanconi anemia is an autosomal recessive disorder with diverse clinical symptoms, including developmental anomalies, bone marrow failure, and early occurrence of malignancies. A minimum of 8 FA genes have been identified.

UOM: 1 * 100 µl

Tilbud