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Image Unavailable-BOSSBS-11997R-HRP

Anti-DDAH1 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Codice catalogo: (BOSSBS-11997R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-11997R-HRP
Codice articolo locale: BOSSBS-11997R-HRP
Descrizione: DDAH, a dimethylarginine dimethylaminohydrolase, hydrolyzes dimethyl arginine (ADMA) and monomethyl arginine (MMA), both inhibitors of nitric oxide synthases, and may be involved in in-vivo modulation of nitric oxide production (1,2). Impairment of DDAH causes ADMA accumulation and a reduction in cGMP generation (3). DDAH II, the predominant DDAH isoform in endothelial cells, facilitates the induction of nitric oxide synthesis by all-trans-Retinoic acid (atRA) (4). DDAH proteins are highly expressed in colon, kidney, stomach and liver tissues (1).
UOM: 1 * 100 µl
Image Unavailable-A14832.06

Elaidic acid ≥98%

Fornitore: Thermo Fisher Scientific
Descrizione: Elaidic acid ≥98%

MSDS Certificati

Image Unavailable-EHERC10934700

Caffeic acid

Codice catalogo: (EHERC10934700)
Fornitore: EHRENSTORFER
Codice articolo fornitore: C10934700
Codice articolo locale: EHERC10934700
Descrizione: Caffeic acid
UOM: 1 * 0,1 g
Image Unavailable-ICNA0210479705

Caffeic acid ≥98%, yellow powder

Fornitore: MP Biomedicals
Descrizione: Caffeic acid is used as an anti-oxidant.

Image Unavailable-SPCMC1466-12KGBL

Acido trans-1,2-diamminocicloesan-N,N,N',N'-tetracetico monoidrato ≥98%, per analisi

Codice catalogo: (SPCMC1466-12KGBL)
Fornitore: Spectrum Chemical
Codice articolo fornitore: C1466-12KGBL
Codice articolo locale: SPCMC1466-12KGBL
Descrizione: (1,2-Cyclohexylenedinitrilo)tetraacetic Acid, Reagent is an alkyl-substituted amino acid that functions as a chelating agent. This ingredient's source is synthetic. It appears as a solid and is partially soluble in cold water. Its reagent grade means this is the highest quality commercially available for this chemical and that the American Chemical Society has not officially set any specifications for this material.
UOM: 1 * 12 kg
Image Unavailable-BOSSBS-11785R-CY3

Anti-SPG21 Rabbit Polyclonal Antibody (Cy3®)

Codice catalogo: (BOSSBS-11785R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-11785R-CY3
Codice articolo locale: BOSSBS-11785R-CY3
Descrizione: Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11785R-A647

Anti-SPG21 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Codice catalogo: (BOSSBS-11785R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-11785R-A647
Codice articolo locale: BOSSBS-11785R-A647
Descrizione: Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
UOM: 1 * 100 µl
Image Unavailable-BNC040638-500

Anti-FGF23 Mouse Monoclonal Antibody (CF405S) [clone: FGF23/638]

Fornitore: Biotium
Descrizione: Fibroblast growth factor-1 (FGF-1), also designated acidic FGF, and fibroblast growth factor-2 (FGF-2), also designated basic FGF, are members of a family of growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin. Additional members of the FGF family include the oncogenes FGF-3 (Int2) and FGF-4 (hst/Kaposi), FGF-5, FGF-6, FGF-7 (KGF), FGF-8 (AIGF), FGF-9 (GAF) and FGF-10 through FGF-23. Members of the FGF family share 30-55% amino acid sequence identity and similar gene structure, and are capable of transforming cultured cells when overexpressed in trans- fected cells. Cellular receptors for FGFs are members of a second multigene family, including four tyrosine kinases designated Flg (FGFR-1), Bek (FGFR-L), TKF and FGFR-3.

Image Unavailable-BOSSBS-8333R-A488

Anti-RDH13 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Codice catalogo: (BOSSBS-8333R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-8333R-A488
Codice articolo locale: BOSSBS-8333R-A488
Descrizione: RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-11785R

Anti-SPG21 Rabbit Polyclonal Antibody

Codice catalogo: (BOSSBS-11785R)
Fornitore: Bioss
Codice articolo fornitore: BS-11785R
Codice articolo locale: BOSSBS-11785R
Descrizione: Maspardin is a 308 amino acid cytoplasmic protein that is widely expressed. Belonging to the AB hydrolase superfamily, Maspardin colocalizes with CD4 on endosomal/trans-Golgi network. It is thought that Maspardin may act as a negative regulatory factor in CD4-dependent T-cell activation. Defects in the gene encoding Maspardin are the result of hereditary spastic paraplegia autosomal recessive type 21 (also designated Mast syndrome), an autosomal recessive neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. The gene encoding Maspardin is encoded by human chromosome 15, which houses over 700 genes and comprises nearly 3% of the human genome.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13454R-CY5

Anti-GMEB1 Rabbit Polyclonal Antibody (Cy5®)

Codice catalogo: (BOSSBS-13454R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-13454R-CY5
Codice articolo locale: BOSSBS-13454R-CY5
Descrizione: GMEB-1 is a 573 amino acid protein that contains one SAND domain and is a member of the KDWK family of combinatorial transcription modulators. Localized to both the cytoplasm and the nucleus, GMEB-1 forms a heterodimer with GMEB-2 (Glucocorticoid modulatory element-binding protein 2) and, once associated with GMEB-2, plays a key role in parvovirus DNA replication. In addition, GMEB-1 functions alone as a trans-acting factor that, by binding to glucocorticoid modulatory elements (GMEs) in TAT (tyrosine aminotransferase) promoters, increases intracellular sensitivity to glucocorticoid concentrations. GMEB-1 also interacts with initiator procaspases and, via this interaction, can inhibit caspase-induced apoptosis. Due to alternative splicing events, GMEB-1 is expressed as two isoforms.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8333R-CY3

Anti-RDH13 Rabbit Polyclonal Antibody (Cy3®)

Codice catalogo: (BOSSBS-8333R-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-8333R-CY3
Codice articolo locale: BOSSBS-8333R-CY3
Descrizione: RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8333R-CY5

Anti-RDH13 Rabbit Polyclonal Antibody (Cy5®)

Codice catalogo: (BOSSBS-8333R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-8333R-CY5
Codice articolo locale: BOSSBS-8333R-CY5
Descrizione: RDH13, also known as all-trans and 9-cis retinol dehydrogenase 13 or SDR7C3, is a 331 amino acid mitochondrial protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, mostly in eye, pancreas, placenta and lung, RDH13 localizes on the outer side of the inner mitochondrial membrane. Related to microsomal retinoid oxidoreductase RDH11, RDH13 is considered to be a major enzyme among the RDH family of proteins. Catalytically active, RDH13 recognizes retinoids as substrates and may function in retinoic acid production. RDH13 may function to protect the mitochondria against oxidative stress. Leber congenital amaurosis (LCA) type 3, an inherited autosomal recessive retinal disease, has been associated with defects of RDH13. LCA represents the most common genetic cause of congenital visual impairment in infants and children.
UOM: 1 * 100 µl
Image Unavailable-B22928.14

Acido trans-1,2-diamminocicloesan-N,N,N',N'-tetracetico monoidrato 98%

Fornitore: Thermo Fisher Scientific
Descrizione: Acido trans-1,2-diamminocicloesan-N,N,N',N'-tetracetico monoidrato 98%

MSDS Certificati

Image Unavailable-BNC940638-500

Anti-FGF23 Mouse Monoclonal Antibody (CF594) [clone: FGF23/638]

Fornitore: Biotium
Descrizione: Fibroblast growth factor-1 (FGF-1), also designated acidic FGF, and fibroblast growth factor-2 (FGF-2), also designated basic FGF, are members of a family of growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin. Additional members of the FGF family include the oncogenes FGF-3 (Int2) and FGF-4 (hst/Kaposi), FGF-5, FGF-6, FGF-7 (KGF), FGF-8 (AIGF), FGF-9 (GAF) and FGF-10 through FGF-23. Members of the FGF family share 30-55% amino acid sequence identity and similar gene structure, and are capable of transforming cultured cells when overexpressed in trans- fected cells. Cellular receptors for FGFs are members of a second multigene family, including four tyrosine kinases designated Flg (FGFR-1), Bek (FGFR-L), TKF and FGFR-3.

Image Unavailable-BNC880638-100

Anti-FGF23 Mouse Monoclonal Antibody (CF488A) [clone: FGF23/638]

Fornitore: Biotium
Descrizione: Fibroblast growth factor-1 (FGF-1), also designated acidic FGF, and fibroblast growth factor-2 (FGF-2), also designated basic FGF, are members of a family of growth factors that stimulate proliferation of cells of mesenchymal, epithelial and neuroectodermal origin. Additional members of the FGF family include the oncogenes FGF-3 (Int2) and FGF-4 (hst/Kaposi), FGF-5, FGF-6, FGF-7 (KGF), FGF-8 (AIGF), FGF-9 (GAF) and FGF-10 through FGF-23. Members of the FGF family share 30-55% amino acid sequence identity and similar gene structure, and are capable of transforming cultured cells when overexpressed in trans- fected cells. Cellular receptors for FGFs are members of a second multigene family, including four tyrosine kinases designated Flg (FGFR-1), Bek (FGFR-L), TKF and FGFR-3.

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