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Masterflex+Single-use
Numéro de catalogue:
(BOSSBS-2980R-HRP)
Fournisseur:
Bioss
Description:
Binds both single-stranded and double-stranded DNA and promotes ATP-independent annealing of complementary single-stranded DNAs and D-loop formation in superhelical double-stranded DNA. May play a role in maintenance of genomic integrity.
UOM:
1 * 100 µl
Numéro de catalogue:
(732-2590)
Fournisseur:
Thermo Fisher Scientific
Description:
VersiPlates comprise strips of eight tubes linked to each other forming the familiar 12×8 or 96-well ANSI/SBS format. The small tear points between strips enable a single strip or as many as required for the individual experiment to be separated.
UOM:
1 * 25 ST
Numéro de catalogue:
(BOSSBS-6634R-A750)
Fournisseur:
Bioss
Description:
Involved in global genome nucleotide excision repair (GG-NER) by acting as damage sensing and DNA-binding factor component of the XPC complex. Has only a low DNA repair activity by itself which is stimulated by RAD23B and RAD23A. Has a preference to bind DNA containing a short single-stranded segment but not to damaged oligonucleotides. This feature is proposed to be related to a dynamic sensor function: XPC can rapidly screen duplex DNA for non-hydrogen-bonded bases by forming a transient nucleoprotein intermediate complex which matures into a stable recognition complex through an intrinsic single-stranded DNA-binding activity. The XPC complex is proposed to represent the first factor bound at the sites of DNA damage and together with other core recognition factors, XPA, RPA and the TFIIH complex, is part of the pre-incision (or initial recognition) complex. The XPC complex recognises a wide spectrum of damaged DNA characterised by distortions of the DNA helix such as single-stranded loops, mismatched bubbles or single-stranded overhangs. The orientation of XPC complex binding appears to be crucial for inducing a productive NER. XPC complex is proposed to recognise and to interact with unpaired bases on the undamaged DNA strand which is followed by recruitment of the TFIIH complex and subsequent scanning for lesions in the opposite strand in a 5'-to-3' direction by the NER machinery. Cyclobutane pyrimidine dimers (CPDs) which are formed upon UV-induced DNA damage esacpe detection by the XPC complex due to a low degree of structural perurbation. Instead they are detected by the UV-DDB complex which in turn recruits and cooperates with the XPC complex in the respective DNA repair. <i>in vitro</i>, the XPC:RAD23B dimer is sufficient to initiate NER; it preferentially binds to cisplatin and UV-damaged double-stranded DNA and also binds to a variety of chemically and structurally diverse DNA adducts.
UOM:
1 * 100 µl
Numéro de catalogue:
(738-1005)
Fournisseur:
Cytiva (Formerly Pall Lab)
Description:
Microplaque, tapis de scellage, Tapis de scellage (96 puits) , Feuille individuelle/tapis/strip, Garniture de bouchon pour incubation, Garniture de bouchon pour incubation
UOM:
1 * 5 ST
Fournisseur:
Metro International
Description:
Étagère, Supports d'étagères pour montage sur poteau, largeur 530 mm, simple, chromé
Numéro de catalogue:
(BOSSBS-13224R-A750)
Fournisseur:
Bioss
Description:
FUBP1 Regulates MYC expression by binding to a single-stranded far-upstream element (FUSE) upstream of the MYC promoter. May act both as activator and repressor of transcription. FUBP2 Binds to the dendritic targeting element and may play a role in mRNA trafficking. Part of a ternary complex that binds to the downstream control sequence (DCS) of the pre-mRNA. Mediates exon inclusion in transcripts that are subject to tissue-specific alternative splicing. May interact with single-stranded DNA from the far-upstream element (FUSE). May activate gene expression. Also involved in degradation of inherently unstable mRNAs that contain AU-rich elements (AREs) in their 3'-UTR, possibly by recruiting degradation machinery to ARE-containing mRNAs.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-2279R-A750)
Fournisseur:
Bioss
Description:
This gene encodes a single-pass type I transmembrane protein, which is a subunit of the endoplasmic reticulum membrane protein complex (EMC). Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
UOM:
1 * 100 µl
Numéro de catalogue:
(ROCK200-403-141)
Fournisseur:
Rockland Immunochemicals
Description:
Anti-beta-2-Microglobulin antibody is suitable for western blotting to detect a single band of the expected apparent molecular weight and for ELISA. Researchers should determine optimal titers for applications that are not stated below.
UOM:
1 * 500 µG
Numéro de catalogue:
(BWTEBWC3R-M30200)
Fournisseur:
BW TECHNOLOGIES GMBH
Description:
Système de détection de gaz, CO
UOM:
1 * 1 ST
New Product
Fournisseur:
Merck
Description:
FocusLiner™ inlet liners are designed with wool plug to promote the rapid vaporisation of the entire sample, minimise mass discrimination, and prevent non-volatile material from entering the column. It incorporates a unique design to prevent the shifting of the wool plug during repeated injections or sudden inlet pressure changes. These liners are suitable for Agilent, Perkinelmer, Shimadzu, Finnigan, Varian and Thermo scientific equipped with split/splitless inlets.
Numéro de catalogue:
(ENZOALX2018500020)
Fournisseur:
ENZO LIFE SCIENCES
Description:
Produced in <i>E. coli</i>. Human Ang-1 (angiopoietin-1) is a single, non-glycosylated polypeptide chain containing 480 amino acids (20 to 498)
UOM:
1 * 20 µG
New Product
Fournisseur:
Brady
Description:
These B-7569 GHS/CLP chemical labels are white with pre-printed red diamond(s).
Numéro de catalogue:
(BOSSBS-7210R-A350)
Fournisseur:
Bioss
Description:
CD45 is a family of single chain transmembraneous glycoproteins consisting of at least four isoforms (220, 205, 190, 180 kDa) which share a common large intracellular domain. Their extracellular domains are heavily glycosylated. The different isoforms are produced by alternative messenger RNA splicing of three exons of a single gene on chromosome 1. CD45 is expressed on cells of the human hematopoietic lineage (including hematopoietic stem cells) with the exception of mature red cells. It is not detected on differentiated cells of other tissues. It is likely that CD45 plays an important role in signal transduction, inhibition or upregulation of various immunological functions. recognising a common epitope on all of the isoforms are termed CD45 whilst those recognising only individual isoforms are termed CD45RA or CD45RO etc.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-7210R-HRP)
Fournisseur:
Bioss
Description:
CD45 is a family of single chain transmembraneous glycoproteins consisting of at least four isoforms (220, 205, 190, 180 kDa) which share a common large intracellular domain. Their extracellular domains are heavily glycosylated. The different isoforms are produced by alternative messenger RNA splicing of three exons of a single gene on chromosome 1. CD45 is expressed on cells of the human hematopoietic lineage (including hematopoietic stem cells) with the exception of mature red cells. It is not detected on differentiated cells of other tissues. It is likely that CD45 plays an important role in signal transduction, inhibition or upregulation of various immunological functions. recognising a common epitope on all of the isoforms are termed CD45 whilst those recognising only individual isoforms are termed CD45RA or CD45RO etc.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13227R-A488)
Fournisseur:
Bioss
Description:
FUNDC1 is a 155 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC1 maps to human chromosome Xp11.3 and mouse chromosome X A1.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13227R-A750)
Fournisseur:
Bioss
Description:
FUNDC1 is a 155 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC1 maps to human chromosome Xp11.3 and mouse chromosome X A1.2. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
UOM:
1 * 100 µl
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