FTCD Mouse Monoclonal Antibody [Kloon ID: UMLBI122]

The protein encoded by this gene is a bifunctional enzyme that channels 1-carbon units from formiminoglutamate, a metabolite of the histidine degradation pathway, to the folate pool. Mutations in this gene are associated with glutamate formiminotransferase deficiency. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2009]

Carrier-free (BSA/glycerol-free) FTCD mouse monoclonal antibody, clone UMLBI122

LCHC1

Homo sapiens formimidoyltransferase cyclodeaminase (FTCD), transcript variant B, mRNA.

10841

O95954

Unconjugated

Histidine metabolism, Metabolic pathways, One carbon pool by folate

Histidine metabolism, Metabolic pathways, One carbon pool by folate

IHC 1:100~200

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

FTCD

https://www.ncbi.nlm.nih.gov/gene/?term=10841

https://www.uniprot.org/uniprot/O95954