Aminomethyltransferase (AMT) (N-term) Rabbit Polyclonal Antibody
Other products for "AMT"
Specifications
Product Data | |
Applications | WB |
Recommended Dilution | Western blot: 1:50 - 1:100. ELISA: 1:1,000. |
Reactivities | Human |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | KLH conjugated synthetic peptide selected from the N-terminal region of human AMT |
Specificity | This antibody detects Aminomethyltransferase at N-term. |
Formulation | PBS with 0.09% (W/V) sodium azide State: Liquid Ig fraction |
Concentration | lot specific |
Purification | Prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS |
Storage | Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing. |
Stability | Shelf life: one year from despatch. |
Gene Name | Homo sapiens aminomethyltransferase (AMT), transcript variant 1 |
Database Link | |
Background | The enzyme system for cleavage of glycine (glycine cleavage system; EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase; MIM 238300), H protein (a lipoic acid-containing protein; MIM 238330), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase; MIM 238331). Glycine encephalopathy (GCE; MIM 605899) may be due to a defect in any one of these enzymes. |
Synonyms | AMT, GCST, GCVT |
Note | Molecular weight: 43946 Da |
Reference Data | |
Protein Pathways | Glycine, serine and threonine metabolism, Metabolic pathways, Nitrogen metabolism, One carbon pool by folate |
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