Esta buscando: N-Carbobenzoxy-L-leucine

Numero del catalogo: (BOSSBS-9407R)

Proveedor: Bioss

Descripción: The small leucine-rich proteoglycan (SLRP) family of proteins contains various proteins such as Decorin, Biglycan, Fibromodulin, Keratocan, Lumican, Osteoadherin and Osteoglycin. These proteins all have similar functions as they all mediate extracellular matrix organization and act as binding partners of TGF beta. Osteoglycin, which also may be designated osteoinductive factor (OIF), is a secreted protein detected in bone tissues. Osteoglycin induces the formation of bone in conjunction with either TGF-beta-1 or TGF-beta-2. The precursor form of the OGN gene product, designated Mimecan, is subject to in situ proteolytic cleavage to yield the mature Osteoglycin.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-5425R-CY7)

Proveedor: Bioss

Descripción: MAX protein is a member of the basic helix-loop-helix leucine zipper (bHLHZ) family of transcription factors. It is able to form homodimers and heterodimers with other family members, which include Mad, Mxi1 and Myc. Myc is an oncoprotein implicated in cell proliferation, differentiation and apoptosis. The homodimers and heterodimers compete for a common DNA target site (the E box) and rearrangement among these dimer forms provides a complex system of transcriptional regulation. Mutations of this gene have been reported to be associated with hereditary pheochromocytoma. A pseudogene of this gene is located on the long arm of chromosome 7. Alternative splicing results in multiple transcript variants.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-2661R-CY7)

Proveedor: Bioss

Descripción: MD1 is a 28 kDa molecule that is associated at the cell surface with RP105 (CD180). RP105 is a leucine-rich repeat (LRR) molecule that is expressed on B lymphocytes. It was first identified by a mAb that protects spleen B cells from irradiation-induced apoptosis. LRR proteins, such as Toll receptors, have a role in innate immunity. MD1 is primarily expressed by B cells, dendritic cells and monocytes, and promotes the recognition of, and subsequent signaling by LPS in the innate immune system. MD1 does not have any homology to other molecules. MD1 when expressed alone behaves as a secretory protein. Expression of MD1 in a cell increases the expression of RP105.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-11282R)

Proveedor: Bioss

Descripción: EVC is an autosomal skeletal dysplasia caused by mutations in the EVC and EVC2 genes. Found in developing ribs, heart, kidney and lung, the EVC gene is responsible for normal development of the face, limbs, teeth and nails. The protein expressed by the EVC gene is an intracellular component of the hedgehog signal pathway that contains a leucine zipper and transmembrane domain. Defects in the EVC gene can lead to short-limb dwarfism, ectodermal dysplasia and cardiac anomalies such as irregular atrioventricular septum development. Additionally, the EVC gene has been implicated in Weyers acrodental dysostosis, an autosomal dominant disease characterized by facial abnormalities and limb defects.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-7134R-CY5)

Proveedor: Bioss

Descripción: This gene encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX), which interacts with histone deacetylase, core histones, and other histone-associated proteins. In mouse, the encoded protein binds to the putative leucine zipper domain of macroH2A1.2, a variant H2A histone that is enriched on inactivated X chromosomes. The BTB/POZ domain of this protein has been shown in other proteins to mediate transcriptional repression and to interact with components of histone deacetylase co-repressor complexes. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-7134R-CY7)

Proveedor: Bioss

Descripción: This gene encodes a protein that may modulate the transcriptional repression activities of death-associated protein 6 (DAXX), which interacts with histone deacetylase, core histones, and other histone-associated proteins. In mouse, the encoded protein binds to the putative leucine zipper domain of macroH2A1.2, a variant H2A histone that is enriched on inactivated X chromosomes. The BTB/POZ domain of this protein has been shown in other proteins to mediate transcriptional repression and to interact with components of histone deacetylase co-repressor complexes. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008].

UOM: 1 * 100 µl

Promoción

Proveedor: MP Biomedicals

Descripción: Leucine is a branched-chain α-amino acid. Leucine is classified as a hydrophobic amino acid due to its aliphatic isobutyl side chain.

Proveedor: G-Biosciences

Descripción: D(-)-Leucina

Numero del catalogo: (PIER88428)

Proveedor: Thermo Fisher Scientific

Descripción: L(+)-Leucina for SILAC

UOM: 1 * 500 mg

Promoción

Numero del catalogo: (PIER88435)

Proveedor: Thermo Fisher Scientific

Descripción: L-Leucine, (¹³C₆), Pierce™

UOM: 1 * 50 mg

Promoción

Numero del catalogo: (4330-100)

Proveedor: Merck Millipore (Calbiochem‎)

Descripción: L(+)-Leucina, Millipore®

UOM: 1 * 100 g

Promoción

Numero del catalogo: (BOSSBS-11282R-CY3)

Proveedor: Bioss

Descripción: EVC is an autosomal skeletal dysplasia caused by mutations in the EVC and EVC2 genes. Found in developing ribs, heart, kidney and lung, the EVC gene is responsible for normal development of the face, limbs, teeth and nails. The protein expressed by the EVC gene is an intracellular component of the hedgehog signal pathway that contains a leucine zipper and transmembrane domain. Defects in the EVC gene can lead to short-limb dwarfism, ectodermal dysplasia and cardiac anomalies such as irregular atrioventricular septum development. Additionally, the EVC gene has been implicated in Weyers acrodental dysostosis, an autosomal dominant disease characterized by facial abnormalities and limb defects.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (BOSSBS-11282R-CY5)

Proveedor: Bioss

Descripción: EVC is an autosomal skeletal dysplasia caused by mutations in the EVC and EVC2 genes. Found in developing ribs, heart, kidney and lung, the EVC gene is responsible for normal development of the face, limbs, teeth and nails. The protein expressed by the EVC gene is an intracellular component of the hedgehog signal pathway that contains a leucine zipper and transmembrane domain. Defects in the EVC gene can lead to short-limb dwarfism, ectodermal dysplasia and cardiac anomalies such as irregular atrioventricular septum development. Additionally, the EVC gene has been implicated in Weyers acrodental dysostosis, an autosomal dominant disease characterized by facial abnormalities and limb defects.

UOM: 1 * 100 µl

Promoción

Numero del catalogo: (ICNA0219469483)

Proveedor: MP Biomedicals

Descripción: L(+)-Leucina

UOM: 1 * 250 g

Promoción

Proveedor: Novabiochem (Part of Merck)

Descripción: N-Fmoc-L-leucina

Certificados

Numero del catalogo: (BOSSBS-5425R-HRP)

Proveedor: Bioss

Descripción: MAX protein is a member of the basic helix-loop-helix leucine zipper (bHLHZ) family of transcription factors. It is able to form homodimers and heterodimers with other family members, which include Mad, Mxi1 and Myc. Myc is an oncoprotein implicated in cell proliferation, differentiation and apoptosis. The homodimers and heterodimers compete for a common DNA target site (the E box) and rearrangement among these dimer forms provides a complex system of transcriptional regulation. Mutations of this gene have been reported to be associated with hereditary pheochromocytoma. A pseudogene of this gene is located on the long arm of chromosome 7. Alternative splicing results in multiple transcript variants.

UOM: 1 * 100 µl

Promoción