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TGM5 encodes a member of the transglutaminase family. Additionally we are shipping Transglutaminase 5 Proteins (4) and many more products for this protein.
Showing 10 out of 44 products:
Human Polyclonal Transglutaminase 5 Primary Antibody for EIA, IF - ABIN1450065
Candi, Oddi, Terrinoni, Paradisi, Ranalli, Finazzi-Agró, Melino: Transglutaminase 5 cross-links loricrin, involucrin, and small proline-rich proteins in vitro. in The Journal of biological chemistry 2001
Show all 5 references for ABIN1450065
Cow (Bovine) Polyclonal Transglutaminase 5 Primary Antibody for WB - ABIN2783673
Cassidy, van Steensel, Steijlen, van Geel, van der Velden, Morley, Terrinoni, Melino, Candi, McLean: A homozygous missense mutation in TGM5 abolishes epidermal transglutaminase 5 activity and causes acral peeling skin syndrome. in American journal of human genetics 2005
We report both European and non-European families with acral peeling skin syndrome carrying mutations in the TGM5 gene. In 5 patients, we found 3 novel mutations: c.1001+2_1001+3del, c.1171G>A and c.1498C>T.
study concludes polymorphisms of TGM5, PPAP2B (show PPAP2B Antibodies) and PSMA4 (show PSMA4 Antibodies) are not major contributors tonon-small cell lung cancer susceptibility in never-smoking hinese population, this primarily can be attributed to the significantly distinct genetic background of Asian populations from western populations
Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitis.
TGM5 mutations impact epidermal differentiation in acral peeling skin syndrome.
analysis of a recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndrome
Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.
transglutaminase 5 contributes, as a secondary effect, to the hyperkeratotic phenotype in ichthyosis (show LBR Antibodies) (both vulgaris and lamellar) and in psoriasis.
Results demonstrate that transglutaminase 5 is able to induce cell death when intracellularly overexpressed.
Data show that transglutaminase (TGase) 5 is acetylated at the N-terminal end, is active upon treatment with phorbol acetate, and co-localises with vimentin (show VIM Antibodies) intermediate filaments.
Transglutaminase 5 is expressed during hair follicle homeostasis.
This gene encodes a member of the transglutaminase family. The encoded protein catalyzes formation of protein cross-links between glutamine and lysine residues, often resulting in stabilization of protein assemblies. This reaction is calcium dependent. Mutations in this gene have been associated with acral peeling skin syndrome.
, protein-glutamine gamma-glutamyltransferase 5-like
, TGase X
, protein-glutamine gamma-glutamyltransferase 5
, transglutaminase V
, transglutaminase X
, TGase 5