You Searched For: HENKE+SASS+WOLF

Catalog Number: (BOSSBS-15591R-A488)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-15591R-A555)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-15591R-A680)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

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Catalog Number: (630-3521)

Supplier: DISCOVER ECHO

Description: CELLCYTE X™ offers the user the ability to image live cells in real-time from within the incubator. From all of these images, the user can fully understand and review cell kinetic trends at any point in time with user-friendly analysis software.

UOM: 1 * 1 items

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Catalog Number: (BOSSBS-15591R-HRP)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-15591R-CY5)

Supplier: Bioss

Description: 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.

UOM: 1 * 100 µl

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Catalog Number: (PRSI27-333)

Supplier: ProSci Inc.

Description: 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.

UOM: 1 * 100 µG

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Catalog Number: (PRSI30-247)

Supplier: ProSci Inc.

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

UOM: 1 * 100 µG

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Supplier: Thermo Scientific

Description: 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.

Catalog Number: (PRSI56-628)

Supplier: ProSci Inc.

Description: 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.

UOM: 1 * 400 µl

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Catalog Number: (PRSI27-870)

Supplier: ProSci Inc.

Description: 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.

UOM: 1 * 50 µG

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Catalog Number: (PRSI28-729)

Supplier: ProSci Inc.

Description: 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.

UOM: 1 * 100 µG

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Catalog Number: (PRSI25-427)

Supplier: ProSci Inc.

Description: 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.

UOM: 1 * 50 µG

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Catalog Number: (STMC100-0899)

Supplier: STEMCELL Technologies

Description: Human amyloid-β (1 to 42) peptide is a neurotoxic peptide fragment that can oligomerize to form amyloid plaques, thus contributing to the onset of Alzheimer's disease (Paradis <i>et al.</i>; Teplow; Wolfe). These neurotoxic peptide fragments also modulate the expression of Bcl-2 and Bax in human neurons (Paradis <i>et al.</i>).

UOM: 1 * 0,5 mg

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Catalog Number: (HSWA8300066301)

Supplier: HENKE SASS WOLF

Description: Henke-Ject 2tlg. 2ML (2.5ML) eco DISPENSER 1 * 100 items

UOM: 1 * 100 items

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Catalog Number: (HSWA8300065155)

Supplier: HENKE SASS WOLF

Description: Henke-Ject 3tlg. 3ML Luer Lock BULK 1 * 4.000 items

UOM: 1 * 4.000 items

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