Sie suchten nach: HENKE+SASS+WOLF

Artikel-Nr: (BOSSBS-15591R-A750)

Lieferant: Bioss

Beschreibung: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-15591R-A647)

Lieferant: Bioss

Beschreibung: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

VE: 1 * 100 µl

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Artikel-Nr: (630-3521)

Lieferant: DISCOVER ECHO

Beschreibung: CELLCYTE X™ bietet dem Anwender die Möglichkeit, lebende Zellen in Echtzeit vom Inkubator aus abzubilden. Anhand all dieser Bilder kann der Benutzer mit Hilfe einer benutzerfreundlichen Analysesoftware die kinetischen Trends der Zellen zu jedem Zeitpunkt vollständig verstehen und überprüfen.

VE: 1 * 1 ST

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Artikel-Nr: (612-0185)

Lieferant: EHRHARDT SOEHNE

Beschreibung: Syringes, two parts, with Luer, blue graduation.

VE: 1 * 100 ST

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Artikel-Nr: (BOSSBS-15591R-HRP)

Lieferant: Bioss

Beschreibung: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-15591R-CY5)

Lieferant: Bioss

Beschreibung: This gene encodes a protein that is localised to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf-Hirschhorn syndrome, a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8, 15 and 19.

VE: 1 * 100 µl

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Lieferant: SANOCLAV WOLF

Beschreibung: Extern exhaust bottle (KB)

Artikel-Nr: (PRSI27-333)

Lieferant: ProSci Inc.

Beschreibung: Slightly proximal to the Huntington disease locus, the human MSX1 gene is deleted in patients with Wolf-Hirschhorn syndrome. This gene is also called HOX7. The Msx family of vertebrate HOX genes was originally isolated by homology to the Drosophila msh (muscle segment homeo box) gene. This is a candidate gene for human cleft palate.

VE: 1 * 100 µG

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Lieferant: SANOCLAV WOLF

Beschreibung: O-ring

Lieferant: Thermo Scientific

Beschreibung: Thermo Scientific CultiMaxx Shelving Systems are designed for use in Heracell VIOS 250i or Heracell Vios 250i Cleanroom CTS Series CO₂ incubators to support scale-out of Thermo Scientific™ Nunc™ Cell Factory™ systems in cell therapy production and are ideal for use with Wilson Wolf G-Rex® 500M-CS bioreactors, standard Nunc Cell Factory system or the Thermo Scientific™ Nunc™ EasyFill™ Cell Factory™ system, both with 4 layers.

Artikel-Nr: (481-4691)

Lieferant: SANOCLAV WOLF

Beschreibung: Hotplate for heating of the autoclaves of KL- series.

VE: 1 * 1 ST

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Artikel-Nr: (PRSI25-427)

Lieferant: ProSci Inc.

Beschreibung: Zinc finger encoding genes would be good candidates for being involved in the multiple developmental defects associated with chromosomal aneusomy--because of their role as transcriptional regulators, their abundance in the genome and their known association with specific developmental disorders. A zinc finger encoding cDNA (ZNF141) of the C2-H2/KRAB subfamily has been mapped to the 4p- (Wolf-Hirschhorn) syndrome (WHS) chromosome region. ZNF141 was expressed ubiquitously at low levels in the analysed tissue. The identification of a candidate gene for a chromosomal aneusomy syndrome belonging to a class of evolutionary conserved genes will provide options for studying its normal and abnormal expression during mammalian embryogenesis.

VE: 1 * 50 µG

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Artikel-Nr: (PRSI28-729)

Lieferant: ProSci Inc.

Beschreibung: Zinc finger encoding genes would be good candidates for being involved in the multiple developmental defects associated with chromosomal aneusomy--because of their role as transcriptional regulators, their abundance in the genome and their known association with specific developmental disorders. A zinc finger encoding cDNA (ZNF141) of the C2-H2/KRAB subfamily has been mapped to the 4p- (Wolf-Hirschhorn) syndrome (WHS) chromosome region. ZNF141 was expressed ubiquitously at low levels in the analysed tissue. The identification of a candidate gene for a chromosomal aneusomy syndrome belonging to a class of evolutionary conserved genes will provide options for studying its normal and abnormal expression during mammalian embryogenesis.

VE: 1 * 100 µG

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Artikel-Nr: (PRSI30-247)

Lieferant: ProSci Inc.

Beschreibung: The LETM1 is a factor of the mitochondrial K+ homeostasis with a potential role in the Wolf-Hirschhorn syndrome.

VE: 1 * 100 µG

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Lieferant: SANOCLAV WOLF

Beschreibung: Small sterilisers for sterilization in tightened steam and water.

Artikel-Nr: (PRSI56-628)

Lieferant: ProSci Inc.

Beschreibung: This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. The function of the protein has not been determined. Two alternatively spliced variants have been described.

VE: 1 * 400 µl

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