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Beschreibung:   Phloroglucintrimethylether
Artikel-Nr: PROOMM0066.05
VE: 1 * 100 mg
Hersteller-Artikelnummer:: MM0066.05
Lokale Artikelnummer:: PROOMM0066.05
Lieferant: LGC Standards PROMOCHEM



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Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF135 (RING finger protein 135), also known as L13, is a 432 amino acid protein that contains one RING-type zinc finger and one SPRY domain. Via its RING-type zinc finger, RNF135 may play a role in transcriptional regulation and protein degradation events. Defects in the gene encoding RNF135 are the cause of RNF135-related overgrowth syndrome which is characterised by learning disabilities, facial dysmorphism and increased weight and height. Multiple isoforms of RNF135 exist due to alternative splicing events.
Artikel-Nr: BOSSBS-11753R-A750
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-11753R-A750
Lokale Artikelnummer:: BOSSBS-11753R-A750
Lieferant: Bioss



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Beschreibung:   FAM13C1, also known as FAM13C, is a 585 amino acid protein that belongs to the FAM13 family. Existing as three alternatively spliced isoforms, the gene encoding FAM13C1 maps to human chromosome 10, which contains over 800 genes, 135 million nucleotides and makes up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterised by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
Artikel-Nr: BOSSBS-8215R-A680
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-8215R-A680
Lokale Artikelnummer:: BOSSBS-8215R-A680
Lieferant: Bioss



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Image Unavailable
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF135 (RING finger protein 135), also known as L13, is a 432 amino acid protein that contains one RING-type zinc finger and one SPRY domain. Via its RING-type zinc finger, RNF135 may play a role in transcriptional regulation and protein degradation events. Defects in the gene encoding RNF135 are the cause of RNF135-related overgrowth syndrome which is characterized by learning disabilities, facial dysmorphism and increased weight and height. Multiple isoforms of RNF135 exist due to alternative splicing events.
Artikel-Nr: BOSSBS-11753R-CY5
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-11753R-CY5
Lokale Artikelnummer:: BOSSBS-11753R-CY5
Lieferant: Bioss



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Image Unavailable
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF135 (RING finger protein 135), also known as L13, is a 432 amino acid protein that contains one RING-type zinc finger and one SPRY domain. Via its RING-type zinc finger, RNF135 may play a role in transcriptional regulation and protein degradation events. Defects in the gene encoding RNF135 are the cause of RNF135-related overgrowth syndrome which is characterized by learning disabilities, facial dysmorphism and increased weight and height. Multiple isoforms of RNF135 exist due to alternative splicing events.
Artikel-Nr: BOSSBS-11753R-HRP
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-11753R-HRP
Lokale Artikelnummer:: BOSSBS-11753R-HRP
Lieferant: Bioss



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Image Unavailable
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF135 (RING finger protein 135), also known as L13, is a 432 amino acid protein that contains one RING-type zinc finger and one SPRY domain. Via its RING-type zinc finger, RNF135 may play a role in transcriptional regulation and protein degradation events. Defects in the gene encoding RNF135 are the cause of RNF135-related overgrowth syndrome which is characterized by learning disabilities, facial dysmorphism and increased weight and height. Multiple isoforms of RNF135 exist due to alternative splicing events.
Artikel-Nr: BOSSBS-11753R-CY7
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-11753R-CY7
Lokale Artikelnummer:: BOSSBS-11753R-CY7
Lieferant: Bioss



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Beschreibung:   The Apoptosis Activator VI, CD437/AHPN, also referenced under CAS 125316-60-1, modulates Apoptosis. This small molecule/inhibitor is primarily used for Cancer applications.
Artikel-Nr: 178496-5
VE: 1 * 5 mg
Hersteller-Artikelnummer:: 178496-5
Lokale Artikelnummer:: CALB178496-5
Lieferant: Merck Millipore (Calbiochem‎)



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Image Unavailable
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF135 (RING finger protein 135), also known as L13, is a 432 amino acid protein that contains one RING-type zinc finger and one SPRY domain. Via its RING-type zinc finger, RNF135 may play a role in transcriptional regulation and protein degradation events. Defects in the gene encoding RNF135 are the cause of RNF135-related overgrowth syndrome which is characterized by learning disabilities, facial dysmorphism and increased weight and height. Multiple isoforms of RNF135 exist due to alternative splicing events.
Artikel-Nr: BOSSBS-11753R-A350
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-11753R-A350
Lokale Artikelnummer:: BOSSBS-11753R-A350
Lieferant: Bioss



Menge:
 
 
 
   
Image Unavailable
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF135 (RING finger protein 135), also known as L13, is a 432 amino acid protein that contains one RING-type zinc finger and one SPRY domain. Via its RING-type zinc finger, RNF135 may play a role in transcriptional regulation and protein degradation events. Defects in the gene encoding RNF135 are the cause of RNF135-related overgrowth syndrome which is characterized by learning disabilities, facial dysmorphism and increased weight and height. Multiple isoforms of RNF135 exist due to alternative splicing events.
Artikel-Nr: BOSSBS-11753R-A647
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-11753R-A647
Lokale Artikelnummer:: BOSSBS-11753R-A647
Lieferant: Bioss



Menge:
 
 
 
   
Image Unavailable
Beschreibung:   The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF135 (RING finger protein 135), also known as L13, is a 432 amino acid protein that contains one RING-type zinc finger and one SPRY domain. Via its RING-type zinc finger, RNF135 may play a role in transcriptional regulation and protein degradation events. Defects in the gene encoding RNF135 are the cause of RNF135-related overgrowth syndrome which is characterized by learning disabilities, facial dysmorphism and increased weight and height. Multiple isoforms of RNF135 exist due to alternative splicing events.
Artikel-Nr: BOSSBS-11753R-A555
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-11753R-A555
Lokale Artikelnummer:: BOSSBS-11753R-A555
Lieferant: Bioss



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Beschreibung:   Phloroglucintrimethylether, Sigma-Aldrich®
Artikel-Nr: SIAL138827-10G
VE: 1 * 10 g
Hersteller-Artikelnummer:: 138827-10G
Lokale Artikelnummer:: SIAL138827-10G
Lieferant: Sigma-Aldrich



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Beschreibung:   This antibody recognizes a cell surface glycoprotein of 95/115/135 kDa (depending upon the extent of glycosylation), identified as CD43 (Workshop III). 70-90% of T-cell lymphomas and from 22-37% of B-cell lymphomas express CD43. No reactivity has been observed with reactive B-cells. So a B-lineage population that co-expresses CD43 is highly likely to be a malignant lymphoma, especially a low-grade lymphoma, rather than a reactive B-cell population. When CD43 antibody is used in combination with anti-CD20, effective immunophenotyping of the lymphomas in formalin-fixed tissues can be obtained. Co-staining of a lymphoid infiltrate with anti-CD20 and anti-CD43 argues against a reactive process and favors a diagnosis of lymphoma.
Artikel-Nr: BNC680342-100
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BNC680342-100
Lokale Artikelnummer:: BTIUBNC680342-100
Lieferant: Biotium



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Beschreibung:   GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Artikel-Nr: BOSSBS-8409R-A488
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-8409R-A488
Lokale Artikelnummer:: BOSSBS-8409R-A488
Lieferant: Bioss



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Beschreibung:   C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Artikel-Nr: BOSSBS-6384R-A647
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-6384R-A647
Lokale Artikelnummer:: BOSSBS-6384R-A647
Lieferant: Bioss



Menge:
 
 
 
   
Image Unavailable
Beschreibung:   GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Artikel-Nr: BOSSBS-8409R-A680
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-8409R-A680
Lokale Artikelnummer:: BOSSBS-8409R-A680
Lieferant: Bioss



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Image Unavailable
Beschreibung:   C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5% of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Artikel-Nr: BOSSBS-6384R-A750
VE: 1 * 100 µl
Hersteller-Artikelnummer:: BS-6384R-A750
Lokale Artikelnummer:: BOSSBS-6384R-A750
Lieferant: Bioss



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