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Numéro de catalogue: (AIRLACCTR26)
Fournisseur: Air Liquide
Description: Réservoir de stockage cryogénique, Bride pour chariot basculeur, Pour: TR21, TR26
UOM: 1 * 1 ST


Numéro de catalogue: (BRDY170386)
Fournisseur: Brady
Description: M211 Hard case
UOM: 1 * 1 ST


Fournisseur: Avantor Fluid Handling
Description: Ideal adapters for plastic case pump heads.

1 year warranty

Numéro de catalogue: (KWIN100898240)
Fournisseur: FRISTADS KANSAS
Description: Heavy-duty split leather tool belt for carpenters, joiners, fitters etc.
UOM: 1 * 1 ST


Fournisseur: ProAmpac
Description: Sachets en polyester ou en aluminium, thermocollables, trois joints d'étanchéité latéraux, transparents, à haute barrière de 63 microns.

Numéro de catalogue: (BELAH132340000)
Fournisseur: Bel-Art Products, a Part of SP
Description: Hard to pierce pouch offering protection against the danger of being cut by contaminated sharp objects. Convenient for labs, clinics and medical offices. Used with the Poxygrid® safety pouch stand for easy benchtop collection.
UOM: 1 * 200 ST


Numéro de catalogue: (LBES7240106)
Fournisseur: LABORATOIRES ESCULAPE
Description: Contents:
UOM: 1 * 1 ST


Numéro de catalogue: (LBES8205250)
Fournisseur: LABORATOIRES ESCULAPE
Description: Small portable eyewash kit in storage pouch.
UOM: 1 * 1 ST


Fournisseur: S▄DPACK MEDICA
Description: Ces sachets auto-adhésifs avec indicateurs décollables sont fournis avec un papier arrière de 60 g/m² et un couvrant transparent en PET/PP.
Numéro de catalogue: (SIMESP1618)
Fournisseur: Industrial Physics
Description: Accessory for coating tester, Pour: Surface profile and coating thickness gauge, Spare leather pouch
UOM: 1 * 1 ST


Numéro de catalogue: (LPIT172030)
Fournisseur: LP ITALIANA
Description: This PE specimen transport bag is with a document pouch with hole for hanging.
UOM: 1 * 2.000 ST


Numéro de catalogue: (111-1946)
Fournisseur: UVEX
Description: Jugulaire résistante en cuir avec œillets en plastique, longueur réglable, pour casques uvex
UOM: 1 * 10 ST


Numéro de catalogue: (BOSSBS-13597R-A647)
Fournisseur: Bioss
Description: The homeobox protein, HESX1, which is also known as Rathke’s pouch homeobox, HANF, homeodomain transcription factor, and anterior-restricted homeobox protein is a transcription factor that belongs to the homeodomain family of DNA binding proteins. HESX1 is initially expressed in embryonic stem cells and the primitive forebrain, and is essential for normal development of the eyes and other anterior CNS structures, such as the hypothalamus, the pituitary gland and the olfactory bulbs. The homeobox gene Hesx1 is expressed in the anterior visceral endoderm (AVE), anterior axial mesendoderm (AME), and anterior neural ectoderm (ANE) during early embryogenesis. Mutations in the Hesx1 gene are associated with disorders that are comparable with septo-optic dysplasia (SOD). These disorders are characterized by hypoplasia of the optic nerve, various types of forebrain defects and pituitary hormone deficiencies, including hypothyroidism. Hesx1 also acts as a transcriptional repressor of reporter gene constructs in tissue culture assays.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-11722R-A350)
Fournisseur: Bioss
Description: Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin ?1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterized by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt抯 lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-11722R-A680)
Fournisseur: Bioss
Description: Neural crest cell migration to the third and fourth pharyngeal pouches is a critical step in the structural formation of organs that are affected in DiGeorge syndrome. DGCR6 (DiGeorge syndrome critical region 6) is a nuclear protein that plays a role in neural crest cell migration and is located at the DiGeorge syndrome critical region (DGCR) on chromosome 22. Expressed ubiquitously with highest levels in heart, liver and skeletal muscle, DGCR6 shares high homology with the Drosophila gonadal (gdl) protein and with human Laminin 1, both of which are involved in early tissue development. The gene encoding DGCR6, along with other DGCR genes, is deleted in DiGeorge syndrome; a developmental disorder characterised by improper facial, cardiac and palate formation. Upregulation of DGCR6 is implicated in lung and colon adenocarcinomas, as well as in Burkitt lymphoma and lymphocytes transformed by EBV. Due to a duplication of the ancestral DGCR6 locus, there are two functional, highly homologous copies of the DGCR6 gene (designated DGCR6 and DGCR6L) on chromosome 22.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-13597R-FITC)
Fournisseur: Bioss
Description: The homeobox protein, HESX1, which is also known as Rathke’s pouch homeobox, HANF, homeodomain transcription factor, and anterior-restricted homeobox protein is a transcription factor that belongs to the homeodomain family of DNA binding proteins. HESX1 is initially expressed in embryonic stem cells and the primitive forebrain, and is essential for normal development of the eyes and other anterior CNS structures, such as the hypothalamus, the pituitary gland and the olfactory bulbs. The homeobox gene Hesx1 is expressed in the anterior visceral endoderm (AVE), anterior axial mesendoderm (AME), and anterior neural ectoderm (ANE) during early embryogenesis. Mutations in the Hesx1 gene are associated with disorders that are comparable with septo-optic dysplasia (SOD). These disorders are characterized by hypoplasia of the optic nerve, various types of forebrain defects and pituitary hormone deficiencies, including hypothyroidism. Hesx1 also acts as a transcriptional repressor of reporter gene constructs in tissue culture assays.
UOM: 1 * 100 µl


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