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4-(1,3-Oxazol-5-yl)phenol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Chloro-2,6-difluoroanisole
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Bromthiazol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Evans-Blau
Artikel-Nr:
(BOSSBS-9611R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9611R-CY7
Lokale Artikelnummer::
BOSSBS-9611R-CY7
Beschreibung:
CLLD6, is a 196 amino acid protein that contains one B30.2/SPRY domain. Expression of CLLD6 is found at highest levels in heart, skeletal muscle and testis, with lower levels found in thymus, peripheral blood leukocytes, lymph node and bone marrow. Existing as two alternatively spliced isoforms, CLLD6 maps to human chromosome 13, which comprises nearly 4% of human DNA and contains about 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9611R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9611R-CY5
Lokale Artikelnummer::
BOSSBS-9611R-CY5
Beschreibung:
CLLD6, is a 196 amino acid protein that contains one B30.2/SPRY domain. Expression of CLLD6 is found at highest levels in heart, skeletal muscle and testis, with lower levels found in thymus, peripheral blood leukocytes, lymph node and bone marrow. Existing as two alternatively spliced isoforms, CLLD6 maps to human chromosome 13, which comprises nearly 4% of human DNA and contains about 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Tris(N,N-dimethylaminopropyl)amine
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
3,5-Dichloro(trifluoromethoxy)benzene 98%
Artikel-Nr:
(APOSPC9538-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
PC9538-1G
Lokale Artikelnummer::
APOSPC9538-1G
Beschreibung:
2,6-Dimethyl-4-fluorochlorobenzene 98%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-9402R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9402R-A750
Lokale Artikelnummer::
BOSSBS-9402R-A750
Beschreibung:
CARKD is a 347 amino acid protein that belongs to the YjeF family and exists as three alternatively spliced isoforms. Containing one YjeF C-terminal domain, CARKD is encoded by a gene that maps to human chromosome 13q34. Chromosome 13 contains around 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is quite deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9402R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9402R-CY7
Lokale Artikelnummer::
BOSSBS-9402R-CY7
Beschreibung:
CARKD is a 347 amino acid protein that belongs to the YjeF family and exists as three alternatively spliced isoforms. Containing one YjeF C-terminal domain, CARKD is encoded by a gene that maps to human chromosome 13q34. Chromosome 13 contains around 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is quite deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9402R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9402R-CY3
Lokale Artikelnummer::
BOSSBS-9402R-CY3
Beschreibung:
CARKD is a 347 amino acid protein that belongs to the YjeF family and exists as three alternatively spliced isoforms. Containing one YjeF C-terminal domain, CARKD is encoded by a gene that maps to human chromosome 13q34. Chromosome 13 contains around 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is quite deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9402R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9402R-A555
Lokale Artikelnummer::
BOSSBS-9402R-A555
Beschreibung:
CARKD is a 347 amino acid protein that belongs to the YjeF family and exists as three alternatively spliced isoforms. Containing one YjeF C-terminal domain, CARKD is encoded by a gene that maps to human chromosome 13q34. Chromosome 13 contains around 114 million base pairs and 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is quite deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
5-Fluorisatosäureanhydrid
Lieferant:
BLD PHARMATECH GMBH
Beschreibung:
5-Brom-2-fluor-m-xylol 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-Bromo-3-fluorophenylacetonitrile
Artikel-Nr:
(ABCAAB39418-100)
Lieferant:
Abcam
Hersteller-Artikelnummer::
AB39418-100
Lokale Artikelnummer::
ABCAAB39418-100
Beschreibung:
Anti-IL-13 receptor alpha 1 Mouse Monoclonal Antibody [clone: GM1E7]
VE:
1 * 100 µG
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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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