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tert-Butyl+2-(ethylamino)acetate
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tert-Butyl+2-(ethylamino)acetate
Lieferant:
Alfa Aesar
Beschreibung:
(±)-1,2-Hexandiol ≥97%
Artikel-Nr:
(BOSSBS-15313R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15313R-FITC
Lokale Artikelnummer::
BOSSBS-15313R-FITC
Beschreibung:
C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15317R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15317R-CY5
Lokale Artikelnummer::
BOSSBS-15317R-CY5
Beschreibung:
C9orf163 (chromosome 9 open reading frame 163) is a 203 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15313R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15313R-CY7
Lokale Artikelnummer::
BOSSBS-15313R-CY7
Beschreibung:
C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15343R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15343R-FITC
Lokale Artikelnummer::
BOSSBS-15343R-FITC
Beschreibung:
C9orf79 is a 1445 amino acid single-pass membrane protein that belongs to the FAM75 family. The gene encoding C9orf79 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15343R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15343R-CY3
Lokale Artikelnummer::
BOSSBS-15343R-CY3
Beschreibung:
C9orf79 is a 1445 amino acid single-pass membrane protein that belongs to the FAM75 family. The gene encoding C9orf79 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-12500R-A750)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-12500R-A750
Lokale Artikelnummer::
BOSSBS-12500R-A750
Beschreibung:
The apolipoprotein L gene family maps to a region on chromosome 22 and encodes six highly homologous proteins designated apoL-I, apoL-II, apoL-III, apoL-IV, apoL-V and apoL-VI, all of which function as components of plasma lipoproteins. ApoL-V (apolipoprotein L-V), also known as APOL5, is a 433 amino acid protein that localizes to the cytoplasm and belongs to the apolipoprotein L family. Expressed in a variety of tissues including testis, stomach, uterus and skeletal muscle, apoL-V is thought to affect the movement of lipids in the cytoplasm and may allow the binding of lipids to organelles. Like other members of the apolipoprotein L family, apoL-V is thought to be involved in the development of schizophrenia.
VE:
1 * 100 µl
Lieferant:
COMBI-BLOCKS
Beschreibung:
(S)-2,2'-Dihydroxy-1,1'-binaphthalin-3,3'-diboronsäure
Artikel-Nr:
(BC87)
Lieferant:
G-Biosciences
Hersteller-Artikelnummer::
BC87
Lokale Artikelnummer::
GENOBC87
Beschreibung:
Ellman's reagent is a versatile, water-soluble compound for quantifying free sulfhydryl groups in solution. It reacts with a free sulfhydryl group to yield a mixed disulfide and 2-nitro-5-thiobenzoic acid (NTB), a measurable yellow colored product at 412nm.
Ellman's reagent is very useful as a free sulfhydryl assay reagent due to its high specificity for -SH groups at neutral pH, high molar extinction coefficient and short reaction time.
VE:
1 * 5 g
Artikel-Nr:
(BOSSBS-6264R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-6264R
Lokale Artikelnummer::
BOSSBS-6264R
Beschreibung:
EMP-2 is a 167 amino acid multi-pass membrane protein that contains four-transmembrane domains and belongs to the GAS3/PMP22 (growth arrest-specific-3/peripheral myelin protein-22) family. Localized to lipid raft domains in the plasma membrane, EMP-2 regulates the expression of several target proteins and is necessary for blastocyst implantation in the uterine endometrium. Specifically, EMP-2 mediates blastocyst implantation by controlling the cell membrane expression of MHC and glycosylphosphatidylinositol-anchored proteins, as well as Integrins and caveolin-1. In adult tissues, EMP-2 is expressed in heart, lung, ovary and intestine, while fetal expression is highest in kidney, brain and liver. Overexpression of EMP-2 is associated with endometrial adenocarcinoma, suggesting a possible role for EMP-2 in tumorigenesis.
VE:
1 * 100 µl
Artikel-Nr:
(EHERC20004400)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C20004400
Lokale Artikelnummer::
EHERC20004400
Beschreibung:
2,2',3,5'-Tetrachlorbiphenyl (PCB Nr. 44)
VE:
1 * 25 mg
Artikel-Nr:
(EHERC20008500)
Lieferant:
EHRENSTORFER
Hersteller-Artikelnummer::
C20008500
Lokale Artikelnummer::
EHERC20008500
Beschreibung:
2,2',3,4,4'-Pentachlorbiphenyl (PCB Nr. 85)
VE:
1 * 10 mg
Artikel-Nr:
(PROOCIL-PCB-179-C)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-179-C
Lokale Artikelnummer::
PROOCIL-PCB-179-C
Beschreibung:
2,2',3,3',5,6,6'-Heptachlorbiphenyl (PCB Nr. 179)
VE:
1 * 5 mg
Artikel-Nr:
(PROOCIL-PCB-133-C)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-133-C
Lokale Artikelnummer::
PROOCIL-PCB-133-C
Beschreibung:
2,2',3,3',5,5'-Hexachlorbiphenyl (PCB Nr. 133)
VE:
1 * 5 mg
Artikel-Nr:
(PROOCIL-PCB-170-C)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-170-C
Lokale Artikelnummer::
PROOCIL-PCB-170-C
Beschreibung:
2,2',3,3',4,4',5-Heptachlorbiphenyl (PCB Nr. 170)
VE:
1 * 5 mg
Artikel-Nr:
(PROOCIL-PCB-172-C)
Lieferant:
LGC Standards PROMOCHEM
Hersteller-Artikelnummer::
CIL-PCB-172-C
Lokale Artikelnummer::
PROOCIL-PCB-172-C
Beschreibung:
2,2',3,3',4,5,5'-Heptachlorbiphenyl (PCB Nr. 172)
VE:
1 * 5 mg
Preis auf Anfrage
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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.
Dieses Produkt kann nur an eine Lieferadresse versandt werden die über die entsprechende Lizenzen verfügt. Für weitere Hilfe bitte kontaktieren Sie Ihr VWR Vertriebszentrum.
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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