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Insert+plates+and+inserts
Numéro de catalogue:
(BOSSBS-8346R-A750)
Fournisseur:
Bioss
Description:
FGFR1OP2 belongs to the SIKE family. The FGFR1OP2 (FGFR1 oncogene partner 2) gene was identified through its involvement in a fusion with the FGFR1 gene. FGFR1OP2 may be involved in the wound healing pathway. It is expressed in bone marrow, spleen and thymus. A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterised by myeloid hyperplasia, eosinophilia and T cell or B cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15206R-CY3)
Fournisseur:
Bioss
Description:
C5orf45 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf45 gene product has been provisionally designated C5orf45 pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8671R-A555)
Fournisseur:
Bioss
Description:
Key component of the cytosolic iron-sulfur protein assembly (CIA) complex, a multiprotein complex that mediates the incorporation of iron-sulfur cluster into apoproteins specifically involved in DNA metabolism and genomic integrity. In the CIA complex, MMS19 acts as an adapter between early-acting CIA components and a subset of cellular target iron-sulfur proteins such as ERCC2/XPD, FANCJ and RTEL1, thereby playing a key role in nucleotide excision repair (NER) and RNA polymerase II (POL II) transcription. As part of the mitotic spindle-associated MMXD complex, plays a role in chromosome segregation, probably by facilitating iron-sulfur cluster assembly into ERCC2/XPD. Indirectly acts as a transcriptional coactivator of estrogen receptor (ER), via its role in iron-sulfur insertion into some component of the TFIIH-machinery.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9500R-HRP)
Fournisseur:
Bioss
Description:
Hemostasis following tissue injury involves the deployment of essential plasma procoagulants (prothrombin, and factors X, IX, V, and VIII), which are involved in a blood coagulation cascade that leads to the formation of insoluble fibrin clots and the promotion of platelet aggregation (1-3). Coagulation factor IX (plasma thromboplastic component, F9, F.IX, HEMB) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor (3,4). Factor XIa mediated proteolytic cleavage of factor IX generates factor IXa, an active serine protease composed of a 145 amino acid light chain and a 236 amino acid catalytic heavy chain, linked through disulfide bonds (5). Genetic alterations at the Factor IX locus such as point mutations, insertions and deletions, can lead to hemophilia B, also known as Christmas disease (6).
UOM:
1 * 100 µl
Fournisseur:
LIOFILCHEM S.R.L.
Description:
Lames flexibles double faces gélosées. Mode d'emploi: <B>1.</B> Dévisser le bouchon contenant la lame gélosée. Conserver le flacon dans l'autre main et appliquer la lame gélosée sur la surface à analyser en faisant une légère pression ou <B>1 bis.</B> Appliquer directement sur le milieu l'écouvillon si vous avez fait un prélèvement par écouvillonnage ou <B>1 ter.</B> Plonger la lame gélosée dans le liquide à analyser.<B> 2.</B> Introduire la lame dans le flacon et revisser. Mettre à l'étuve à 37° pendant 24/48 heures. Pour la recherche des levures prolonger l'incubation de 24/48 heures à 25/30 °C.
Numéro de catalogue:
(1.08641.0001)
Fournisseur:
Merck
Description:
Souvent utilisée pour savoir si un conteneur rempli de liquides (hydrophobes) tels que des carburants moteur ou des huiles peut contenir de l'eau sous la couche d'huile. La pâte est appliquée sur une tige de niveau quelconque, qui est ensuite plongée dans le conteneur. La pâte change de couleur au contact de l'eau.
UOM:
1 * 150 g
Numéro de catalogue:
(BOSSBS-8346R-A555)
Fournisseur:
Bioss
Description:
FGFR1OP2 belongs to the SIKE family. The FGFR1OP2 (FGFR1 oncogene partner 2) gene was identified through its involvement in a fusion with the FGFR1 gene. FGFR1OP2 may be involved in the wound healing pathway. It is expressed in bone marrow, spleen and thymus. A chromosomal aberration involving FGFR1OP2 may be a cause of stem cell myeloproliferative disorder (MPD). Insertion ins(12;8)(p11;p11p22) with FGFR1. MPD is characterized by myeloid hyperplasia, eosinophilia and T cell or B cell lymphoblastic lymphoma. In general it progresses to acute myeloid leukemia. The fusion protein FGFR1OP2-FGFR1 may exhibit constitutive kinase activity and be responsible for the transforming activity.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8315R)
Fournisseur:
Bioss
Description:
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The FAM53C gene product has been provisionally designated FAM53C pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8344R-CY7)
Fournisseur:
Bioss
Description:
FCHSD1 is a 690 amino acid protein that contains one FCH domain and two SH3 domains. FCHSD1 exists as three isoforms as a result of alternative splicing events. The gene encoding FCHSD1 maps to chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8344R-CY3)
Fournisseur:
Bioss
Description:
FCHSD1 is a 690 amino acid protein that contains one FCH domain and two SH3 domains. FCHSD1 exists as three isoforms as a result of alternative splicing events. The gene encoding FCHSD1 maps to chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15202R-CY5)
Fournisseur:
Bioss
Description:
C5orf34 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf34 gene product has been provisionally designated C5orf34 pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9483R-FITC)
Fournisseur:
Bioss
Description:
With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15201R-CY3)
Fournisseur:
Bioss
Description:
C5orf24 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf24 gene product has been provisionally designated C5orf24 pending further characterization.
UOM:
1 * 100 µl
Fournisseur:
HUBER
Description:
Thermostats de bain à circulation avec bains en polycarbonate ou en acier inoxydable, simples à utiliser et adaptés à diverses applications telles que : contrôle de la température des échantillons, analyses, essais de matériaux ou contrôle des aliments. Les appareils offrent une grande stabilité thermique et sont dotés d'une protection contre les surchauffes et les niveaux bas adaptée à la classe de sécurité III/FL (DIN 12876) pour une utilisation avec des fluides inflammables. Une puissante pompe de pression/aspiration assure une circulation et une homogénéité de température optimales dans le bain et permet aussi de contrôler la température d'applications externes à l'aide d'un adaptateur de pompe (accessoire). Il y a une gamme d'accessoires comprenant des inserts, des plates-formes à réglage variable, des couvercles de bain, des sondes ainsi que des tuyaux, des fluides de contrôle de la température et divers adaptateurs.
Numéro de catalogue:
(700-0001)
Fournisseur:
Thermo Fisher Scientific
Description:
PSF, closures with platinum cured silicone inserts.
UOM:
1 * 1 ST
Fournisseur:
ELTEN GMBH
Description:
Chaussures de sécurité antistatiques légères, allure sport, sans cuir, en microfibres, avec inserts en maille, équipées d'une languette rembourrée et d'une semelle antidérapante en PU/PU bi-densité Fun.
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est toujours affiché et vous avez besoin d'aide, s'il vous plaît appelez-nous au 016 385 011
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