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58K Golgi protein(N-Term)/FTCD AntibodyPeptide-affinity purified goat antibody

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AF1003a 0.1mg 400 ul 7-10 days $ 325.00 Add to cart
  • Specification
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58K Golgi protein(N-Term)/FTCD Antibody - Product info

Other AccessionNP_996848
ReactivityHuman
Concentration100ug/200ul
IsotypeIgG

58K Golgi protein(N-Term)/FTCD Antibody - Additional info

Other Names
FTCD; LCHC1; formiminotransferase cyclodeaminase; formimidoyltransferase cyclodeaminase
Format
0.5 mg IgG/ml in Tris saline (20mM Tris pH7.3, 150mM NaCl), 0.02% sodium azide, with 0.5% bovine serum albumin
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
58K Golgi protein(N-Term)/FTCD Antibody is for research use only and not for use in diagnostic or therapeutic procedures.

58K Golgi protein(N-Term)/FTCD Antibody - Application data

  • AF1003a (0.03 µg/ml) staining of Human Liver lysate (35 µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.

  • AF1003a (3.8 µg/ml) staining of paraffin embedded Human Liver. Steamed antigen retrieval with citrate buffer pH 6, AP-staining.

58K Golgi protein(N-Term)/FTCD Antibody - Related products

AP6646b: FTCD Antibody (C-term)

AP6646c: FTCD Antibody (Center)

RI12079: FTCD predesign siRNA

BP6646b: FTCD Antibody (C-term) Blocking Peptide

BP6646c: FTCD Antibody (Center) Blocking Peptide

AT2112a: FTCD Antibody (monoclonal) (M01)

AT2113a: FTCD Antibody (monoclonal) (M02)

AF1003a: 58K Golgi protein(N-Term)/FTCD Antibody

AF1003b: 58KGolgi protein(Internal)/FTCD Antibody

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Provided below are standard protocols that you may find useful for product applications.

BACKGROUND

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.

REFERENCES

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia. Jugessur A, et al. PLoS One, 2010 Jul 9. PMID 20634891. Variation at the NFATC2 Locus Increases the Risk of Thiazolinedinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study. Bailey SD, et al. Diabetes Care, 2010 Jul 13. PMID 20628086. Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. Talmud PJ, et al. Am J Hum Genet, 2009 Nov. PMID 19913121. Transcriptomic and genetic studies identify IL-33 as a candidate gene for Alzheimer's disease. Chapuis J, et al. Mol Psychiatry, 2009 Nov. PMID 19204726. An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1). Franke B, et al. Birth Defects Res A Clin Mol Teratol, 2009 Mar. PMID 19161160.