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BIOSS INC
Artikel-Nr:
(BOSSBS-15298R-HRP)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15298R-HRP
Lokale Artikelnummer::
BOSSBS-15298R-HRP
Beschreibung:
C8ORF59.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9192R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9192R-A680
Lokale Artikelnummer::
BOSSBS-9192R-A680
Beschreibung:
May have a role in spermatogenesis.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-13113R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-13113R-CY5
Lokale Artikelnummer::
BOSSBS-13113R-CY5
Beschreibung:
This gene encodes a member of the ETS family of transcription factors, which are defined by the presence of a conserved ETS DNA-binding domain that recognizes the core consensus DNA sequence GGAA/T in target genes. These proteins function either as transcriptional activators or repressors of numerous genes, and are involved in stem cell development, cell senescence and death, and tumorigenesis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Jul 2011].
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15208R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15208R-A647
Lokale Artikelnummer::
BOSSBS-15208R-A647
Beschreibung:
C5orf49 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 C5orf49 gene product has been provisionally designated C5orf49 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15086R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15086R-CY5
Lokale Artikelnummer::
BOSSBS-15086R-CY5
Beschreibung:
C1r B chain is a serine protease that combines with C1q and C1s to form C1, the first component of the classical pathway of the complement system.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15153R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15153R-CY7
Lokale Artikelnummer::
BOSSBS-15153R-CY7
Beschreibung:
C2orf54 (chromosome 2 open reading frame 54), also known as FLJ22671, MGC150431 or MGC150432, is a 447 amino acid protein that exists as three alternatively spliced isoforms, which are encoded by a gene located on human chromosome 2q37.3. The second largest human chromosome, chromosome 2 consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15198R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15198R-A350
Lokale Artikelnummer::
BOSSBS-15198R-A350
Beschreibung:
C5orf19 is a member of the receptor expression enhancing protein family. Studies of a related gene in mouse suggest that the encoded protein is found in the cell membrane and enhances the function of sweet taste receptors. Alternative splicing results in multiple transcript variants.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15131R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15131R-CY5
Lokale Artikelnummer::
BOSSBS-15131R-CY5
Beschreibung:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf13 gene product has been provisionally designated C22orf13 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-15193R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-15193R-FITC
Lokale Artikelnummer::
BOSSBS-15193R-FITC
Beschreibung:
Representing approximately 6% of the human genome, chromosome 4 contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease. Chromosome 4 reportedly contains the largest gene deserts (regions of the genome with no protein encoding genes) and has one of the two lowest recombination frequencies of the human chromosomes. The C4orf40 gene product has been provisionally designated C4orf40 pending further characterization.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9546R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9546R-CY3
Lokale Artikelnummer::
BOSSBS-9546R-CY3
Beschreibung:
FIBCD1 is a 461 amino acid single-pass membrane protein that contains one fibrinogen C-terminal domain and exists as multiple alternatively spliced isoforms. The gene encoding FIBCD1 maps to human chromosome 9, which contains 145 million base pairs, comprises 4% of the human genome and encodes nearly 900 genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9689R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9689R-A647
Lokale Artikelnummer::
BOSSBS-9689R-A647
Beschreibung:
TWA1 is a 228 amino acid nuclear protein that is highly conserved throughout evolution. TWA1 interacts with Ran BP-M, a protein that is implicated in a diverse array of cellular processes including DNA replication, entry into and exit from mitosis, and the transport of RNA and proteins through the nuclear pore complex. Together, Ran BP-M and TWA1 form a complex with cytoplasmic Muskelin, a mediator of cell spreading. It is thought that this complex plays a role in the Ran GTPase cycle and therefore a potential role in the cell cycle. TWA1 contains a LisH-CTLH motif which is usually found in proteins that are involved in nucleokinesis, chromosome segregation, cell migration and microtubule dynamics. The gene encoding TWA1 maps to human chromosome 20, which comprises approximately 2% of the human genome and contains nearly 63 million bases that encode over 600 genes.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8148R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8148R-A350
Lokale Artikelnummer::
BOSSBS-8148R-A350
Beschreibung:
CHCHD8
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8113R-CY5.5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8113R-CY5.5
Lokale Artikelnummer::
BOSSBS-8113R-CY5.5
Beschreibung:
CCDC127
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8502R-A488)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8502R-A488
Lokale Artikelnummer::
BOSSBS-8502R-A488
Beschreibung:
Involved in the activation cascade of caspases responsible for apoptosis execution. Binding of caspase-9 to Apaf-1 leads to activation of the protease which then cleaves and activates caspase-3. Promotes DNA damage-induced apoptosis in a ABL1/c-Abl-dependent manner. Proteolytically cleaves poly(ADP-ribose) polymerase (PARP). Isoform 2 lacks activity is an dominant-negative inhibitor of caspase-9.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-8327R-FITC)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-8327R-FITC
Lokale Artikelnummer::
BOSSBS-8327R-FITC
Beschreibung:
Participates in the second catalytic step of pre-mRNA splicing, when the free hydroxyl group of exon I attacks the 3'-splice site to generate spliced mRNA and the excised lariat intron. Required for holding exon 1 properly in the spliceosome and for correct AG identification when more than one possible AG exists in 3'-splicing site region. May be involved in the activation of proximal AG. Probably also involved in alternative splicing regulation.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-9551R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9551R-CY3
Lokale Artikelnummer::
BOSSBS-9551R-CY3
Beschreibung:
BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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.
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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