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Anticorps
Numéro de catalogue:
(BOSSBS-15480R-A647)
Fournisseur:
Bioss
Description:
Hho1.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15480R-CY3)
Fournisseur:
Bioss
Description:
Hho1.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-15480R-A680)
Fournisseur:
Bioss
Description:
Hho1.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9004R-A680)
Fournisseur:
Bioss
Description:
SAMD3.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9004R-A647)
Fournisseur:
Bioss
Description:
SAMD3
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-5148R-CY7)
Fournisseur:
Bioss
Description:
Seems to phosphorylate critical substrates that regulate the G1/S phase transition and/or DNA replication. Can phosphorylates MCM2 and MCM3.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-5148R-CY5)
Fournisseur:
Bioss
Description:
Seems to phosphorylate critical substrates that regulate the G1/S phase transition and/or DNA replication. Can phosphorylates MCM2 and MCM3.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9004R-CY7)
Fournisseur:
Bioss
Description:
SAMD3
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9659R-A647)
Fournisseur:
Bioss
Description:
With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and β thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11. The FAM76B gene product has been provisionally designated FAM76B pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9004R-HRP)
Fournisseur:
Bioss
Description:
SAMD3
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-12183R-A555)
Fournisseur:
Bioss
Description:
Voltage-gated K+ channels in the plasma membrane control the repolarization and the frequency of action potentials in neurons, muscles, and other excitable cells. The KV gene family encodes more than 30 genes that comprise the subunits of the K+ channels, and they vary in their gating and permeation properties, subcellular distribution, and expression patterns. Functional KV channels assemble as tetramers consisting of pore-forming alpha-subunits (KV alpha), which include the KV1, KV2, KV3, and KV4 proteins, and accessory or KV beta subunits that modify the gating properties of the coexpressed KV alpha subunits. Differences exist in the patterns of trafficking, biosynthetic processing and surface expression of the major KV1 subunits (KV1.1, KV1.2, KV1.4, KV1.5 and KV1.6) expressed in rat and human brain, suggesting that the individual protein subunits are highly regulated to control for the assembly and formation of functional neuronal channels.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9004R-A350)
Fournisseur:
Bioss
Description:
SAMD3
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9004R-CY3)
Fournisseur:
Bioss
Description:
SAMD3
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9151R-FITC)
Fournisseur:
Bioss
Description:
Functions as an E3 ligase that catalyzes the ubiquitin-mediated degradation of protein kinase C.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9657R-CY5)
Fournisseur:
Bioss
Description:
Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The FAM78B gene product has been provisionally designated FAM78B pending further characterization.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-12142R-CY7)
Fournisseur:
Bioss
Description:
The membranes of myelinating Schwann cells are joined by tight, gap and adherens junctions, all of which are found in regions of noncompact myelin: the paranodal loops, incisures of Schmidt-Lanterman and mesaxons. Tight junctions help establish polarity in mammalian epithelia by forming a physical barrier that separates apical and basolateral membranes. Pals-associated tight junction protein (PATJ), the human homolog of Drosophila Discs Lost, is differentially localized in myelinating Schwann cells. PATJ associates with Claudin-1, CRB1 (a transmembrane protein that plays a role in epithelial cell polarity and photoreceptor development), and Pals1 (a Lin-7 associated protein). The PATJ/Pals1/CRB1 complex can form a tripartite tight junction in epithelial cells crucial to their integrity.
UOM:
1 * 100 µl
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