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Ace+Method+Development+Kits


97,324  results were found

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Catalog Number: (10101-660)

Supplier:  Prosci
Description:   The specific function of PKNOX1 is not yet known.
Catalog Number: (10104-950)

Supplier:  Prosci
Description:   HCLS1 is a substrate for caspase cleavage during apoptosis.
Catalog Number: (10101-386)

Supplier:  Prosci
Description:   ZNF404 may be involved in transcriptional regulation.
Catalog Number: (10101-374)

Supplier:  Prosci
Description:   The exact function of FOXL1 remains unknown.
Catalog Number: (10099-862)

Supplier:  Prosci
Description:   The specific function of FAM82B is not yet known.
Catalog Number: (10102-132)

Supplier:  Prosci
Description:   The specific function of SIX4 is not yet known.
Catalog Number: (10107-954)

Supplier:  Prosci
Description:   The functions of NSF remain unknown.
Catalog Number: (10750-640)

Supplier:  Prosci
Description:   JMJD6 Antibody: The jumonji domain-containing protein (JMJD) family is defined by the presence of the JmjC domain that is observed in several diverse species. JMJD6 was initially identified as a membrane protein that participates in phagocytosis but recent studies have shown that it has other functions when it is expressed in the cytosol and nucleus. JMJD6 is thought to play important roles in regulation of development and differentiation as knockdown experiments in mice resulted in neonatal lethality with severe defects in the morphology of numerous organs. JMJD6 also can catalyze the lysyl-hydroxylation of U2AF65, a protein involved with RNA splicing, suggesting that some of the functions attributed to JMJD6 may be due to its regulatory activity of RNA splicing.
Catalog Number: (10750-776)

Supplier:  Prosci
Description:   VLK Antibody: VLK was identified as a novel protein kinase that was induced after the differentiation of cultured embryonic stem cells into mesendoderm. It has no homologs in invertebrates, but is highly conserved in vertebrate species although it does not belong to any known protein kinase groups. VLK is initially expressed in E-cadherin-positive anterior visceral endoderm and mesendoderm, but its expression is later confined to E-cadherin-negative mesenchyme. It is enriched in the Golgi apparatus and is thought to regulate the rate of protein export from the Golgi. Targeted disruption of VLK in mice leads to a defect in lung development and neonatal lethality. It has been suggested that mutations in VLK may be associated with the allergic condition atopy.
Supplier:  Bioss
Description:   CESK1, also known as CCT8L2 (chaperonin containing TCP1, subunit 8 theta-like 2), is a 557 amino acid protein that localizes to the cytoplasm and is thought to function as a molecular chaperone, possibly assisting protein folding after ATP hydrolysis. CESK1 belongs to the TCP-1 chaperonin family and is encoded by a gene which maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein Bcr-Abl, a potent cell proliferation activator found in several types of leukemias.

Supplier:  Bioss
Description:   CCDC11 is a 514 amino acid protein encode by a gene that maps to human chromosome 18q21.1. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers, and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18.
Catalog Number: (470233-810)

Supplier:  American 3B Scientific
Description:   Impedance converter with high-resistance input for measuring extremely small charges and currents.
Supplier:  Bioss
Description:   FGF22 is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The mouse homolog of this gene was found to be preferentially expressed in the inner root sheath of the hair follicle, which suggested a role in hair development.Fibroblast Growth Factor-22 stimulates the proliferation and activation of cells that express FGF receptor.

Supplier:  Genetex
Description:   Amyloidosis is a heterogeneous group of disorders characterized by extracellular deposition of abnormal protein fibrils, which are derived from different proteins. Almost all patients with amyloidosis have some level of renal disorders. The immunoperoxidase technique has the advantage of being able to detect amyloid in formalin-fixed paraffin embedded tissues and is a very specific method for identifying amyloid fibril proteins. Small and minute amounts of amyloid can be detected with both Amyloid P and Amyloid A (GT20655) antibodies, and thus could allow earlier treatment before organ damage has occurred.
Supplier:  Thermo Scientific Chemicals
Description:   Used as a photographic developer, glass tint, decorative glass colorant, and pigment in plastics, paints, and lacquers.
Supplier:  Thermo Scientific Chemicals
Description:   MDL: MFCD00011354 Beilstein Registry No.: 3902972 Fieser: 1,502 8,261 10,212 11,268 18,193 19,176 20,200 21,233
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