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Image non disponible-BOSSBS-9756R-A680

Anti-ANKRD26 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Description: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD26 (ankyrin repeat domain-containing protein 26) is a 1709 amino acid protein that contains five ANK repeats. Expressed at high level in many tissues, including brain, liver, kidney and heart, ANKRD26 may be phosphorylated upon DNA damage by Atm or ATR. ANKRD26 is also expressed in the arcuate and ventromedial nuclei within the hypothalamus and in the ependyma and the circumventricular organs that act as an interface between the peripheral circulation and the brain. It is suggested that alterations in the gene encoding ANKRD26 may lead to obesity. Three isoforms of ANKRD26 exists due to alternative splicing events.
Numéro de catalogue: BOSSBS-9756R-A680
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-9743R-A680

Anti-ANKLE2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Description: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKLE2 (ankyrin repeat and LEM domain containing 2), also known as LEMD7, is a 938 amino acid single-pass membrane protein containing an ANK repeat and a LEM domain. Existing as two isoforms produced by alternative splicing events, the gene encoding ANKLE2 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.
Numéro de catalogue: BOSSBS-9743R-A680
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-7962R-CY3

Anti-ANKRD12 Rabbit Polyclonal Antibody (Cy3®)

Description: Ankyrin repeats containing cofactors may recruit histone deacetylases to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation.
Numéro de catalogue: BOSSBS-7962R-CY3
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-7962R-HRP

Anti-ANKRD12 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Description: Ankyrin repeats containing cofactors may recruit histone deacetylases to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation.
Numéro de catalogue: BOSSBS-7962R-HRP
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-7962R-A350

Anti-ANKRD12 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Description: Ankyrin repeats containing cofactors may recruit histone deacetylases to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation.
Numéro de catalogue: BOSSBS-7962R-A350
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-6709R-A680

Anti-CaI-PLA2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Description: Catalyzes the release of fatty acids from phospholipids. It has been implicated in normal phospholipid remodeling, nitric oxide-induced or vasopressin-induced arachidonic acid release and in leukotriene and prostaglandin production. May participate in fas mediated apoptosis and in regulating transmembrane ion flux in glucose-stimulated B-cells. Has a role in cardiolipin (CL) deacylation. Required for both speed and directionality of monocyte MCP1/CCL2-induced chemotaxis through regulation of F-actin polymerisation at the pseudopods. Isoform ankyrin-iPLA2-1 and isoform ankyrin-iPLA2-2, which lack the catalytic domain, are probably involved in the negative regulation of iPLA2 activity.
Numéro de catalogue: BOSSBS-6709R-A680
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-7962R-CY7

Anti-ANKRD12 Rabbit Polyclonal Antibody (Cy7®)

Description: Ankyrin repeats containing cofactors may recruit histone deacetylases to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation.
Numéro de catalogue: BOSSBS-7962R-CY7
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-9743R-CY5.5

Anti-ANKLE2 Rabbit Polyclonal Antibody (Cy5.5®)

Description: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKLE2 (ankyrin repeat and LEM domain containing 2), also known as LEMD7, is a 938 amino acid single-pass membrane protein containing an ANK repeat and a LEM domain. Exsiting as two isoforms produced by alternative splicing events, the gene encoding ANKLE2 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.
Numéro de catalogue: BOSSBS-9743R-CY5.5
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-9743R-A488

Anti-ANKLE2 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Description: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKLE2 (ankyrin repeat and LEM domain containing 2), also known as LEMD7, is a 938 amino acid single-pass membrane protein containing an ANK repeat and a LEM domain. Exsiting as two isoforms produced by alternative splicing events, the gene encoding ANKLE2 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.
Numéro de catalogue: BOSSBS-9743R-A488
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-0289R-CY5

Anti-Neurofascin Rabbit Polyclonal Antibody (Cy5®)

Description: Cell adhesion, ankyrin-binding protein which may be involved in neurite extension, axonal guidance, synaptogenesis, myelination and neuron-glial cell interactions.
Numéro de catalogue: BOSSBS-0289R-CY5
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-0289R-A555

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

Description: Cell adhesion, ankyrin-binding protein which may be involved in neurite extension, axonal guidance, synaptogenesis, myelination and neuron-glial cell interactions.
Numéro de catalogue: BOSSBS-0289R-A555
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-0289R-A647

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

Description: Cell adhesion, ankyrin-binding protein which may be involved in neurite extension, axonal guidance, synaptogenesis, myelination and neuron-glial cell interactions.
Numéro de catalogue: BOSSBS-0289R-A647
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-9755R-A750

Anti-ANKRD26 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Description: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD26 (ankyrin repeat domain-containing protein 26) is a 1709 amino acid protein that contains five ANK repeats. Expressed at high level in many tissues, including brain, liver, kidney and heart, ANKRD26 may be phosphorylated upon DNA damage by Atm or ATR. ANKRD26 is also expressed in the arcuate and ventromedial nuclei within the hypothalamus and in the ependyma and the circumventricular organs that act as an interface between the peripheral circulation and the brain. It is suggested that alterations in the gene encoding ANKRD26 may lead to obesity. Three isoforms of ANKRD26 exists due to alternative splicing events.
Numéro de catalogue: BOSSBS-9755R-A750
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-9745R-A350

Anti-ANKRD13B Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Description: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes can lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD13B (ankyrin repeat domain 13B) is a 626 amino acid protein that contains two ANK repeats and three ubiquitin-interacting motif (UIM) repeats. Conserved in dog, cow, mouse and rat, ANKRD13B exists as two alternatively spliced isoforms. The gene that encodes ANKRD13B maps to human chromosome 17, which makes up over 2.5% of the human genome, with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. BRCA1 is recognized as a genetic determinant of early onset breast cancer. Chromosome 17 is also linked to neurofibromatosis, dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease.
Numéro de catalogue: BOSSBS-9745R-A350
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-9748R-A350

Anti-ANKRD22 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Description: Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. 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 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.
Numéro de catalogue: BOSSBS-9748R-A350
UOM: 1 * 100 µl
Fournisseur: Bioss
Image non disponible-BOSSBS-7962R-A680

Anti-ANKRD12 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Description: Ankyrin repeats containing cofactors may recruit histone deacetylases to the p160 coactivators/nuclear receptor complex to inhibit ligand-dependent transactivation.
Numéro de catalogue: BOSSBS-7962R-A680
UOM: 1 * 100 µl
Fournisseur: Bioss
545 - 560 of 282 845