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Omschrijving: MS4A6A is a member of the membrane-spanning 4A gene family and may be involved in signal transduction as a component of a multimeric receptor complex. There are three named isoforms.
Catalogus nummer: BOSSBS-13692R-FITC
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: <p><span style="color:black">TriLink’s CleanCap® AG (3′ OMe) CleanScript™ IVT kit provides essential components for mRNA synthesis using co-transcriptional capping by in vitro transcription (IVT). The kit components are sufficient to run 25 of 100 µl reactions following our recommended IVT protocol with co-transcriptional capping. It includes a cap analog, modified and unmodified nucleotides, IVT enzymes including CleanScribe RNA polymerase, 10X CleanScript IVT reaction buffer, and a linearized FLuc DNA control template.</span></p>
Catalogus nummer: SOLUK-7413-25
UOM: 1 * 100 µl
Leverancier: TriLink BioTechnologies

New Product


Omschrijving: This gene includes 11 exons spanning 25 kb and maps to a region of chromosome 16 that is sometimes deleted in breast and prostrate cancer. The second intron contains an apparently intronless gene, C16orf3, that is transcribed in the opposite orientation. This gene is a putative tumor suppressor gene.
Catalogus nummer: BOSSBS-6009R
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: MS4A6A is a member of the membrane-spanning 4A gene family and may be involved in signal transduction as a component of a multimeric receptor complex. There are three named isoforms.
Catalogus nummer: BOSSBS-13692R-A680
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: Non ionic detergent efficiently separates hydrophilic proteins from membrane spanning, hydrophobic proteins without altering biological activity.
Catalogus nummer: J575-1G
UOM: 1 * 1 g
Leverancier: VWR Chemicals

MSDS


Omschrijving: Span® 80
Catalogus nummer: ROTH9426.1
UOM: 1 * 250 g
Leverancier: Roth Carl


Omschrijving: BAI1, a p53-target gene, encodes brain-specific angiogenesis inhibitor, a seven-span transmembrane protein and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities and may also play a role in angiogenesis.
Catalogus nummer: BOSSBS-7514R-CY7
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: solute carrier family 24, member 5 ( SLC24A5 protein ) is a member of the potassium-dependent sodium/calcium exchanger family andencodes an intracellular membrane protein with 2 large hydrophilic loops and 2 sets of multiple transmembrane- spanning segments. Sequence variation in this gene has been associated with differences in skin pigmentation.
Catalogus nummer: BOSSBS-0496R
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: BAI1, a p53-target gene, encodes brain-specific angiogenesis inhibitor, a seven-span transmembrane protein and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities and may also play a role in angiogenesis.
Catalogus nummer: BOSSBS-7514R-CY3
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
Catalogus nummer: BOSSBS-8042R-A750
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
Catalogus nummer: BOSSBS-8042R-HRP
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: Aluminiumlegering Laboral.
Catalogus nummer: 241-0032
UOM: 1 * 2 ST
Leverancier: VWR Collection


Omschrijving: <p><span style="color:black"> BspQI (isoschizomers: SapI, PciSI and LguI) is a Type IIS restriction enzyme known for its unique cleavage properties. It recognizes asymmetric DNA sequences, cleaves the double-stranded DNA outside of the recognition site, and generates a 5′ overhang.</span></p>
Catalogus nummer: SOLUE-0097-S
UOM: 1 * 1 EA
Leverancier: TriLink BioTechnologies

New Product


Omschrijving: The Major facilitator superfamily consists of presumed carbohydrate transporters with 10-12 membrane-spanning domains. Belonging to the facilitator superfamily, HIAT1 is a 490 amino acid multi-pass membrane protein that may function as a sugar transporter and is expressed in adult and embryonic brain. The HIAT1 gene was first observed while analyzing for active genes in neonatal mouse hippocampus. The gene encoding HIAT1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. Stickler syndrome, Parkinsons, schizophrenia, familial adenomatous polyposis, Gaucher disease and Usher syndrome are also associated with chromosome 1.
Catalogus nummer: BOSSBS-8042R-A350
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: DUSP2 is a dual-specific thr/tyr phosphatase that is a physiologically relevant MAP kinase phosphatase. The gene is located on 2q11.2-q11 and contains 4 exons that span approximately 2.3kb. Under specific stress conditions, p53 regulates transcription of PAC1 through a new p53-binding site, and that PAC1 is necessary and sufficient for p53-mediated apoptosis.
Catalogus nummer: BOSSBS-7609R-CY5
UOM: 1 * 100 µl
Leverancier: Bioss


Omschrijving: BAI1, a p53-target gene, encodes brain-specific angiogenesis inhibitor, a seven-span transmembrane protein and is thought to be a member of the secretin receptor family. Brain-specific angiogenesis proteins BAI2 and BAI3 are similar to BAI1 in structure, have similar tissue specificities and may also play a role in angiogenesis.
Catalogus nummer: BOSSBS-7514R-A488
UOM: 1 * 100 µl
Leverancier: Bioss


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