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Artikel-Nr:
(BOSSBS-15342R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15342R-A350
Lokale Artikelnummer::
BOSSBS-15342R-A350
Beschreibung:
Chromosome 9 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. The C9orf78 gene product has been provisionally designated C9orf78 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15328R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15328R-A488
Lokale Artikelnummer::
BOSSBS-15328R-A488
Beschreibung:
Chromosome 9 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. The C9orf40 gene product has been provisionally designated C9orf40 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15337R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15337R-A680
Lokale Artikelnummer::
BOSSBS-15337R-A680
Beschreibung:
Chromosome 9 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. The C9orf66 gene product has been provisionally designated C9orf66 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15328R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15328R-A555
Lokale Artikelnummer::
BOSSBS-15328R-A555
Beschreibung:
Chromosome 9 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. The C9orf40 gene product has been provisionally designated C9orf40 pending further characterisation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9747R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9747R
Lokale Artikelnummer::
BOSSBS-9747R
Beschreibung:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases 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 characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, 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-15318R)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15318R
Lokale Artikelnummer::
BOSSBS-15318R
Beschreibung:
C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 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 characterized 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:
(USBI041830-BIOTIN)
Lieferant:
US Biological
Hersteller-Artikelnummer::
041830-BIOTIN
Lokale Artikelnummer::
USBI041830-BIOTIN
Beschreibung:
Anti-SLC22A2 Rabbit Polyclonal Antibody (Biotin)
VE:
1 * 200 µl
Lieferant:
Sigma-Aldrich
Beschreibung:
Cystaminiumdichlorid, Sigma-Aldrich®
Artikel-Nr:
(REST32420)
Lieferant:
Restek
Hersteller-Artikelnummer::
32420
Lokale Artikelnummer::
REST32420
Beschreibung:
Contains eight components, those are 2-chlorobiphenyl, 2,3-dichlorobiphenyl, 2,4,5-trichlorobiphenyl, 2,2',4,4'-tetrachlorobiphenyl, 2,2',3',4,6-pentachlorobiphenyl, 2,2',4,4',5,6'-hexachlorobiphenyl, 2,2',3,3',4,4',6-heptachlorobiphenyl and 2,2',3,3',4,5',6,6'-octachlorobiphenyl.
VE:
1 * 1 mL
Lieferant:
PRECISION DYNAMICS TIMEM
Beschreibung:
These thin labels are suitable for use with microscopy slides.
Lieferant:
FRISTADS KANSAS
Beschreibung:
Diese Hosen bestehen aus XA32 Material, welches aus 99% Polyester und 1% leitfähigen Fasern gefertigt ist. Bei den Fasern handelt es sich um Endlosfilamentfasern, das heißt, die Kleidungsstücke geben weder Partikel noch Fasern ab. Die Carbonfilamente erzeugen eine gute statische Entladung, verhindern so eine statische Aufladung und minimieren die triboelektrische Anziehung von Partikeln und Fasern. Dadurch sind die Kleidungsstücke sehr gut für Tätigkeiten wie beispielsweise das Lackieren von Fahrzeugen geeignet.
Artikel-Nr:
(BOSSBS-9489R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9489R-FITC
Lokale Artikelnummer::
BOSSBS-9489R-FITC
Beschreibung:
C9orf46 is a 147 amino acid transmembrane protein. The gene encoding C9orf46 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 characterized 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-9656R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9656R-A647
Lokale Artikelnummer::
BOSSBS-9656R-A647
Beschreibung:
Chromosome 9 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 characterized 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. The FAM78A gene product has been provisionally designated FAM78A pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(PRSI7593)
Lieferant:
ProSci Inc.
Hersteller-Artikelnummer::
7593
Lokale Artikelnummer::
PRSI7593
Beschreibung:
Interleukin-22 (IL-22) is a cytokine important for the modulation of tissue responses during inflammation. Unlike the distantly related IL-10, IL-22 does not inhibit the production of proinflammatory cytokines in monocytes in response to LPS, but it has some inhibitory effects on IL-4 production from Th2 T cells. IL-22 is expressed by both the adaptive arm of the immune system such as CD4 T cell subsets including Th17 cells, as well as by innate lymphocytes such as NK and LTi-like cells. IL-22 is highly expressed in several chronic inflammatory conditions, and studies suggest that IL-22 plays both inflammatory and protective roles.
VE:
1 * 100 µG
Artikel-Nr:
(BOSSBS-15317R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15317R-HRP
Lokale Artikelnummer::
BOSSBS-15317R-HRP
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-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15313R-CY5
Lokale Artikelnummer::
BOSSBS-15313R-CY5
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
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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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