Wyszukano: Kwas (2,4-dimetoksyfenylo)octowy

Numer katalogowy: (BOSSBS-15591R-A647)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (BOSSBS-15591R-A750)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (BOSSBS-15591R)

Producent: Bioss

Opis: This gene encodes a protein that is localized 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. [provided by RefSeq, Oct 2009].

j.m.: 1 * 100 µl

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Numer katalogowy: (BOSSBS-15591R-CY7)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (BOSSBS-15591R-CY3)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (BOSSBS-15591R-HRP)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-15591R-CY5)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-15591R-A555)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-15591R-A350)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-15591R-A488)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

Wyprzedaż

Numer katalogowy: (BOSSBS-15591R-A680)

Producent: Bioss

Opis: 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.

j.m.: 1 * 100 µl

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Numer katalogowy: (PRSI27-870)

Producent: ProSci Inc.

Opis: WHSC1 encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4.

j.m.: 1 * 50 µG

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Numer katalogowy: (PRSI27-333)

Producent: ProSci Inc.

Opis: 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.

j.m.: 1 * 100 µG

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Producent: Thermo Scientific

Opis: 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.

Numer katalogowy: (PRSI28-729)

Producent: ProSci Inc.

Opis: 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.

j.m.: 1 * 100 µG

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Numer katalogowy: (PRSI25-427)

Producent: ProSci Inc.

Opis: 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.

j.m.: 1 * 50 µG

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