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Image Unavailable-BOSSBS-11822R-CY3

Anti-CSAD Rabbit Polyclonal Antibody (Cy3®)

Codice catalogo: (BOSSBS-11822R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-11822R-CY3
Codice articolo locale: BOSSBS-11822R-CY3
Descrizione: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8319R-A680

Anti-HDHD2B Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Codice catalogo: (BOSSBS-8319R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-8319R-A680
Codice articolo locale: BOSSBS-8319R-A680
Descrizione: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11822R-CY5

Anti-CSAD Rabbit Polyclonal Antibody (Cy5®)

Codice catalogo: (BOSSBS-11822R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-11822R-CY5
Codice articolo locale: BOSSBS-11822R-CY5
Descrizione: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8319R-A350

Anti-LHPP Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Codice catalogo: (BOSSBS-8319R-A350)
Fornitore: Bioss
Codice articolo fornitore: BS-8319R-A350
Codice articolo locale: BOSSBS-8319R-A350
Descrizione: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-A750

Anti-Gcn1l1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Codice catalogo: (BOSSBS-13315R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-13315R-A750
Codice articolo locale: BOSSBS-13315R-A750
Descrizione: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
Image Unavailable-P5455-250GR

HEPES (Acido 2-[4-(2-idrossietil)-1-piperazinil]-etansolfonico), in polvere reagente per coltura cellulare, not sterile

Fornitore: Biowest
Descrizione: HEPES (Acido 2-[4-(2-idrossietil)-1-piperazinil]-etansolfonico), in polvere reagente per coltura cellulare, not sterile

MSDS Certificati

Image Unavailable-BOSSBS-13315R-A555

Anti-GCN1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Codice catalogo: (BOSSBS-13315R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-13315R-A555
Codice articolo locale: BOSSBS-13315R-A555
Descrizione: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-FITC

Anti-GCN1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Codice catalogo: (BOSSBS-13315R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-13315R-FITC
Codice articolo locale: BOSSBS-13315R-FITC
Descrizione: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13315R-A647

Anti-GCN1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Codice catalogo: (BOSSBS-13315R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-13315R-A647
Codice articolo locale: BOSSBS-13315R-A647
Descrizione: GCN1L1 is a 2,671 amino acid protein that is ubiquitously expressed and belongs to the GCN1 family. Functioning as a translation activator, GCN1L1 interacts with IMPACT to regulproteinate GCN2 kinase activity. GCN1L1 contains 24 HEAT repeats and is encoded by a gene that maps to human chromosome 12q24.23. Chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8319R-A647

Anti-LHPP Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Codice catalogo: (BOSSBS-8319R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-8319R-A647
Codice articolo locale: BOSSBS-8319R-A647
Descrizione: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8319R-A750

Anti-HDHD2B Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Codice catalogo: (BOSSBS-8319R-A750)
Fornitore: Bioss
Codice articolo fornitore: BS-8319R-A750
Codice articolo locale: BOSSBS-8319R-A750
Descrizione: LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. 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.
UOM: 1 * 100 µl
Product Image-441476L

HEPES (Acido 2-[4-(2-idrossietil)-1-piperazinil]-etansolfonico) ≥99.5%

Codice catalogo: (441476L)
Fornitore: VWR Chemicals
Codice articolo locale: VWRC441476L
Descrizione: Hepes è un tampone ampiamente utilizzato in studi biologici. In terreni di coltura cellulare è impiegato come sostituto del tampone bicarbonato a una concentrazione di 25 mM o come un supplemento al tampone bicarbonato (concentrazione del 10 - 15 mm).
UOM: 1 * 1 kg

MSDS Certificati


Image Unavailable-APOSOR911625-25G

tert-Butyl-5-norbornene-2-carboxylate (endo and exo mixture) 95%

Fornitore: Apollo Scientific
Descrizione: tert-Butyl-5-norbornene-2-carboxylate (endo and exo mixture) 95%

Image Unavailable-BOSSBS-8130R

Anti-CCDC38 Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-8130R)
Fornitore: Bioss
Codice articolo fornitore: BS-8130R
Codice articolo locale: BOSSBS-8130R
Descrizione: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
Image Unavailable-APOSBI8181-250G

HEPES (Acido 2-[4-(2-idrossietil)-1-piperazinil]-etansolfonico) free acid ≥99.5%, ultrapuro

Fornitore: Apollo Scientific
Descrizione: Biological buffer - useful range 6.8 - 8.2

Image Unavailable-BOSSBS-11822R-CY7

Anti-CSAD Rabbit Polyclonal Antibody (Cy7®)

Codice catalogo: (BOSSBS-11822R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-11822R-CY7
Codice articolo locale: BOSSBS-11822R-CY7
Descrizione: CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
UOM: 1 * 100 µl
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La disponibilità per questo articolo è limitata, ma potrebbe essere disponibile in un magazzino vicino a voi. Si prega di assicurarsi che si è effettuato l'accesso al sito, in modo che ledisponibilità possano essere visualizzati. Se il call è ancora visualizzato e hai bisogno di assistenza, si prega di telefonare a 1-800-932 - 5000.
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