Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
TCN2 encodes a member of the vitamin B12-binding protein family. Zusätzlich bieten wir Ihnen Transcobalamin II Antikörper (44) und Transcobalamin II Proteine (13) und viele weitere Produktgruppen zu diesem Protein an.
Showing 6 out of 26 products:
Human TCN2 ELISA Kit für 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
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 (zeige MTX1 ELISA Kits) treatment. CONCLUSIONS: The MTHFR (zeige MTHFR ELISA Kits) 677CC and GGH (zeige GGH ELISA Kits) 401TT and CT genotypes were associated with a reduction in the number of MTX (zeige MTX1 ELISA Kits)-related adverse events.
Report TCN2 mutations causing transcobalamin deficiency in an Indian patient.
Although not significant when corrected for multiple testing, eight single nucleotide polymorphisms (SNPs) in two genes, transcobalamin II (TCN2) and the transcobalamin II-receptor (TCblR (zeige CD320 ELISA Kits)), were found to influence several clinical traits of cobalamin deficiency.
In Asian populations, the investigated polymorphisms mapping at TCN2 and CBS (zeige CBS ELISA Kits) genes did not provide any evidence of association with cleft lip/cleftpalate.
TCN2 776C --> G polymorphism is negatively associated with Alzheimer's type dementia, suggesting a protective role against the disease in subjects with the 5, 10-methylenetetrahydrofolate reductase (zeige MTHFR ELISA Kits) 1298AA genotype
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