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Image Unavailable-BOSSBS-11359R-HRP

Anti-RIMS3 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Descripción: Rab 3, a neural/neuroendocrine-specific member of the Rab family, is involved in Ca2+-regulated exocytosis and functions in an inhibitory capacity, controlling the recruitment and pooling of secretory vesicles at the plasma membrane. The Rim (Rab 3 interacting molecule) family of proteins (Rim1, Rim2, Rim3 and Rim4) are multidomain adaptors that regulate Rab 3 activity and sub-sequent neurotransmitter release. Rim3, also known as RIMS3 (regulating synaptic membrane exocytosis 3) or NIM3, is a 308 amino acid member of the Rim family. Localized to the synapse and to cell junctions, Rim3 contains one C2 domain and is thought to play an important role in the regulation of synaptic membrane exocytosis. Rim3, a protein that may be phosphorylated upon DNA damage, is expressed throughout the body with highest levels present in brain tissue.
Numero del catalogo: BOSSBS-11359R-HRP
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11359R-CY5

Anti-RIMS3 Rabbit Polyclonal Antibody (Cy5®)

Descripción: Rab 3, a neural/neuroendocrine-specific member of the Rab family, is involved in Ca2+-regulated exocytosis and functions in an inhibitory capacity, controlling the recruitment and pooling of secretory vesicles at the plasma membrane. The Rim (Rab 3 interacting molecule) family of proteins (Rim1, Rim2, Rim3 and Rim4) are multidomain adaptors that regulate Rab 3 activity and sub-sequent neurotransmitter release. Rim3, also known as RIMS3 (regulating synaptic membrane exocytosis 3) or NIM3, is a 308 amino acid member of the Rim family. Localized to the synapse and to cell junctions, Rim3 contains one C2 domain and is thought to play an important role in the regulation of synaptic membrane exocytosis. Rim3, a protein that may be phosphorylated upon DNA damage, is expressed throughout the body with highest levels present in brain tissue.
Numero del catalogo: BOSSBS-11359R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11359R-A647

Anti-RIMS3 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descripción: Rab 3, a neural/neuroendocrine-specific member of the Rab family, is involved in Ca2+-regulated exocytosis and functions in an inhibitory capacity, controlling the recruitment and pooling of secretory vesicles at the plasma membrane. The Rim (Rab 3 interacting molecule) family of proteins (Rim1, Rim2, Rim3 and Rim4) are multidomain adaptors that regulate Rab 3 activity and sub-sequent neurotransmitter release. Rim3, also known as RIMS3 (regulating synaptic membrane exocytosis 3) or NIM3, is a 308 amino acid member of the Rim family. Localized to the synapse and to cell junctions, Rim3 contains one C2 domain and is thought to play an important role in the regulation of synaptic membrane exocytosis. Rim3, a protein that may be phosphorylated upon DNA damage, is expressed throughout the body with highest levels present in brain tissue.
Numero del catalogo: BOSSBS-11359R-A647
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11705R-A647

Anti-AIP1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descripción: AIP1 (ASK-interacting protein 1), also known as DAB2IP (DAB2 interacting protein), is a 1,189 amino acid protein that localizes to both the membrane and the cytoplasm and contains one Ras-GAP domain, one PH domain and one C2 domain. Expressed at low levels in prostate tissue, AIP1 functions as a Ras GTPase-activating protein that interacts with ASK 1 and, via this interaction, disrupts the association of ASK 1 with an inhibitory 14-3-3 complex, thereby allowing free ASK 1 to function within the cell. AIP1 exists as multiple alternatively spliced isoforms and is down-regulated in prostate cancer tissue, suggesting a role in tumor suppression. Chromosomal aberrations in the gene encoding AIP1 are associated with acute myeloid leukemia (AML), implicating a role for AIP1 fusion proteins in tumorigenesis.
Numero del catalogo: BOSSBS-11705R-A647
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11705R-A350

Anti-AIP1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Descripción: AIP1 (ASK-interacting protein 1), also known as DAB2IP (DAB2 interacting protein), is a 1,189 amino acid protein that localizes to both the membrane and the cytoplasm and contains one Ras-GAP domain, one PH domain and one C2 domain. Expressed at low levels in prostate tissue, AIP1 functions as a Ras GTPase-activating protein that interacts with ASK 1 and, via this interaction, disrupts the association of ASK 1 with an inhibitory 14-3-3 complex, thereby allowing free ASK 1 to function within the cell. AIP1 exists as multiple alternatively spliced isoforms and is down-regulated in prostate cancer tissue, suggesting a role in tumor suppression. Chromosomal aberrations in the gene encoding AIP1 are associated with acute myeloid leukemia (AML), implicating a role for AIP1 fusion proteins in tumorigenesis.
Numero del catalogo: BOSSBS-11705R-A350
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11034R-CY3

Anti-MYBPC1 Rabbit Polyclonal Antibody (Cy3®)

Descripción: MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 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.
Numero del catalogo: BOSSBS-11034R-CY3
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11034R-A350

Anti-MYBPC1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Descripción: MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 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.
Numero del catalogo: BOSSBS-11034R-A350
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11034R-A750

Anti-MYBPC1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Descripción: MYBPC1 is a 1141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1100 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.
Numero del catalogo: BOSSBS-11034R-A750
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11468R-A350

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

Descripción: Nogo is an oligodendrocyte-specific member of the Reticulon family and is a component of CNS white matter that inhibits axon outgrowth, induces collapse of growth cones of chick dorsal root ganglion cells, and inhibits the spreading of 3T3 fibroblasts. Nogo is expressed by oligodendrocytes but not by Schwann cells and associates primarily with the endoplasmic reticulum. Nogo exists in three different splice forms, Nogo-A, -B and -C. NgBR (Nogo-B receptor), also known as nuclear undecaprenyl pyrophosphate synthase 1 homolog, is a 293 amino acid single-pass type I membrane protein that acts as a specific receptor for the amino-terminus of Nogo-B. Through this interaction, NgBR is involved in the regulation of vascular remodeling and angiogenesis. NgBR also enhances Niemann-Pick type C2 protein (NPC2) stabilization. Knockdown of NgBR mRNA leads to decreased NPC2 levels, which results in the hallmarks of NPC2 mutation: increased intracellular cholesterol accumulation and a loss of sterol sensing.
Numero del catalogo: BOSSBS-11468R-A350
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-11468R-CY5

Anti-NGBR Rabbit Polyclonal Antibody (Cy5®)

Descripción: Nogo is an oligodendrocyte-specific member of the Reticulon family and is a component of CNS white matter that inhibits axon outgrowth, induces collapse of growth cones of chick dorsal root ganglion cells, and inhibits the spreading of 3T3 fibroblasts. Nogo is expressed by oligodendrocytes but not by Schwann cells and associates primarily with the endoplasmic reticulum. Nogo exists in three different splice forms, Nogo-A, -B and -C. NgBR (Nogo-B receptor), also known as nuclear undecaprenyl pyrophosphate synthase 1 homolog, is a 293 amino acid single-pass type I membrane protein that acts as a specific receptor for the amino-terminus of Nogo-B. Through this interaction, NgBR is involved in the regulation of vascular remodeling and angiogenesis. NgBR also enhances Niemann-Pick type C2 protein (NPC2) stabilization. Knockdown of NgBR mRNA leads to decreased NPC2 levels, which results in the hallmarks of NPC2 mutation: increased intracellular cholesterol accumulation and a loss of sterol sensing.
Numero del catalogo: BOSSBS-11468R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-TCIAB5651-250MG

21-[(tert-Butoxycarbonyl)amino]-4,7,10,13,16,19-hexaoxaheneicosanoic acid ≥98.0% (by HPLC)

Descripción: 21-[(tert-Butoxycarbonyl)amino]-4,7,10,13,16,19-hexaoxaheneicosanoic acid ≥98.0% (by HPLC)
Numero del catalogo: TCIAB5651-250MG
UOM: 1 * 250 mg
Proveedor: TCI
Image Unavailable-TCIAB4025-5G

Boc-L-homoserine ≥98.0% (by HPLC, titration analysis)

Descripción: Boc-L-homoserine ≥98.0% (by HPLC, titration analysis)
Numero del catalogo: TCIAB4025-5G
UOM: 1 * 5 g
Proveedor: TCI
Image Unavailable-TCIAB5367-1G

cis-4-(Boc-amino)cyclohexanol ≥98.0% (por GC)

Descripción: cis-4-(Boc-amino)cyclohexanol ≥98.0% (por GC)
Numero del catalogo: TCIAB5367-1G
UOM: 1 * 1 g
Proveedor: TCI
Image Unavailable-H62473.03

(R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid 95%

Descripción: (R)-2-((tert-Butoxycarbonyl)amino)-3,3-dimethylbutanoic acid 95%
Numero del catalogo: H62473.03
UOM: 1 * 1 g
Proveedor: Thermo Fisher Scientific

Certificados


Image Unavailable-APOSOR42214-25G

N-Boc-L-threonine

Descripción: N-Boc-L-threonine
Numero del catalogo: APOSOR42214-25G
UOM: 1 * 25 g
Proveedor: Apollo Scientific
Image Unavailable-TCIAB1638-10G

N-Boc-L-threonine ≥98.0% (by titrimetric analysis)

Descripción: N-Boc-L-threonine ≥98.0% (by titrimetric analysis)
Numero del catalogo: TCIAB1638-10G
UOM: 1 * 10 g
Proveedor: TCI
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