"SANOCLAV WOLF"

Supplier: ProSci Inc.

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.

Supplier: US Biological

Anti-WHSC1L1 Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-WHSC1L1 Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-WHSC1L1 Rabbit Polyclonal Antibody (Biotin)

Supplier: US Biological

Anti-WHSC1L1 Mouse Polyclonal Antibody

Supplier: US Biological

Anti-WHSC1 Rabbit Polyclonal Antibody (Biotin)

Supplier: US Biological

Anti-WHSC1 Mouse Polyclonal Antibody

Supplier: ProSci Inc.

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.

Supplier: Biorbyt

Anti-WHSC1 Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-WHSC1 Rabbit Polyclonal Antibody

Supplier: Biorbyt

Anti-WHSC1 Rabbit Polyclonal Antibody

Supplier: Thermo Scientific

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.

Supplier: Biorbyt

Anti-WHSC1 isoform 3 Rabbit Polyclonal Antibody

Supplier: ProSci Inc.

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.

Supplier: ProSci Inc.

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.

Supplier: Merck

Halloysite nanoclay, Sigma-Aldrich®