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Methyl-4\\\'-brombiphenyl-4-carboxylat
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Methyl-4\\\'-brombiphenyl-4-carboxylat
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Your search request has been modified to limit number of results. Your search was - 4,4-Dimethylcyclohexa-1,5-dienylborons\\\\\\\\u00E4ure+Mononatriumsalz |
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Lieferant:
G-Biosciences
Beschreibung:
SWIFT™ transfer pads are treated with a proprietary electrolyte buffer to enhance Western blot transfer efficiency.
Lieferant:
Sigma-Aldrich
Beschreibung:
Natriumhexanoat, Sigma-Aldrich®
Lieferant:
COMBI-BLOCKS
Beschreibung:
Indazol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3-(4-Ethylphenyl)-3-oxopropanenitrile
Artikel-Nr:
(229-0064)
Lieferant:
BOCHEM
Hersteller-Artikelnummer::
12519
Lokale Artikelnummer::
BOCH12519
Beschreibung:
Messing, vernickelt.
VE:
1 * 1 ST
Lieferant:
CHEMPUR SILANE
Beschreibung:
(Trimethylstannyl)dimethylphenylsilan
Lieferant:
Sigma-Aldrich
Beschreibung:
m-Toluidin, Sigma-Aldrich®
Artikel-Nr:
(BOSSBS-13326R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-CY3
Lokale Artikelnummer::
BOSSBS-13326R-CY3
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
MAPK/ERK Signalling Pathway
Artikel-Nr:
(SWAN0905)
Lieferant:
SWANN MORTON
Hersteller-Artikelnummer::
0905
Lokale Artikelnummer::
SWAN0905
Beschreibung:
Bulbous stainless steel handles for surgical scalpel blades. Individually sleeved.
VE:
1 * 1 ST
Artikel-Nr:
(BOSSBS-11012R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-11012R-A350
Lokale Artikelnummer::
BOSSBS-11012R-A350
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13326R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-HRP
Lokale Artikelnummer::
BOSSBS-13326R-HRP
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13326R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13326R-A680
Lokale Artikelnummer::
BOSSBS-13326R-A680
Beschreibung:
Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The LOC390637 gene product has been provisionally designated LOC390637 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(114-6943)
Lieferant:
HONEYWELL SAFETY
Hersteller-Artikelnummer::
6243854/44
Lokale Artikelnummer::
DALL6243854/44
Beschreibung:
Safety shoes made from suede leather and mesh upper, 3-D lining plus a PU/TPU sole.
VE:
1 * 1 PAAR
Artikel-Nr:
(BOSSBS-4726R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4726R-A680
Lokale Artikelnummer::
BOSSBS-4726R-A680
Beschreibung:
Gross cystic disease is a common premenopausal disorder in which gross cysts are the predominant pathologic lesion. It is characterised by production of a fluid secretion which accumulates in the breast cysts. Gross cystic disease fluid is a pathologic secretion from breast composed of several glycoproteins, including a unique 15 kDa monomer protein, GCDFP 15. The cells within the body that produce GCDFP 15 appear to be restricted primarily to those with apocrine function. Studies have found GCDFP 15 to be a highly specific and sensitive marker for breast cancer.
VE:
1 * 100 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Phthalsäureanhydrid, Sigma-Aldrich®
Preis auf Anfrage
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Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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