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TCN2 encodes a member of the vitamin B12-binding protein family. Additionally we are shipping Transcobalamin II Antibodies (43) and Transcobalamin II Proteins (13) and many more products for this protein.
Showing 4 out of 26 products:
Human TCN2 ELISA Kit for Sandwich ELISA - ABIN422422
Kim, Ahn, Lim, Kim, Kim, Kwon: Daily nutritional dose supplementation with antioxidant nutrients and phytochemicals improves DNA and LDL stability: a double-blind, randomized, and placebo-controlled trial. in Nutrients 2013
tagSNPs in MTHFR (show MTHFR ELISA Kits), MTR (show MTR ELISA Kits), MTRR (show MTRR ELISA Kits), and TCN2 were not associated with NSCLP in our study, but continued exploration, including allele frequency of various populations and molecular mechanism of the gene-gene interactions of the genes, may provide additional insight into NSCLP.
TCN2 (rs1801198, rs9606756) polymorphisms as well as folate deficiency and vitamin B12 deficiency are correlated with Crohn's disease.
The rs9606756[c.67A>G,p.Ile23Val] variant from TCN2 was associated with waist circumference (WC) at nearly genome-wide significance (P = 8.92E-08).
TCN2 polymorphism is associated with ulcerative colitis.
The association of the TCN2 polymorphism with peripheral neuropathy was independent of vitamin B-12 intake.
G/G homozygosity of C776G TC2 and the C/G genotype of the C776G TC2 genegene polymorphism increases the risk of oral cancer
The mutation does not seem to interfere with the function of TC, but the mutation may well explain the low level of holoTC detected by the Abbott assay. The results underscores that mutations of TCN2 have to be considered when implausible holoTC results are obtained.
4 patients with transcobalamin II deficiency were found to have novel mutations, of whom 2 had the same large deletion (homozygous c.1106+1516-1222+1231del). One had c.1107- 347_1222+981delin 364. Another had homozygous c.106C>T. (Q36X).
There were no other associations between single -nucleotide polymorphisms and the efficacy of MTX (show MTX1 ELISA Kits) treatment. CONCLUSIONS: The MTHFR (show MTHFR ELISA Kits) 677CC and GGH (show GGH ELISA Kits) 401TT and CT genotypes were associated with a reduction in the number of MTX (show MTX1 ELISA Kits)-related adverse events.
Report TCN2 mutations causing transcobalamin deficiency in an Indian patient.
study investigated crystallographically the beta-ligand exchange on Cbl bound to transcobalamin (TC) by crystallization of bovine holo-TC in the presence of either cyanide or sulfite
This gene encodes a member of the vitamin B12-binding protein family. This family of proteins, alternatively referred to as R binders, is expressed in various tissues and secretions. This plasma protein binds cobalamin and mediates the transport of cobalamin into cells. This protein and other mammalian cobalamin-binding proteins, such as transcobalamin I and gastric intrisic factor, may have evolved by duplication of a common ancestral gene. Alternative splicing results in multiple transcript variants.
, transcobalamin II
, macrocytic anemia
, transcobalamin II; macrocytic anemia
, vitamin B12-binding protein 2