ARG58881
anti-GLDC antibody
anti-GLDC antibody for ICC/IF,Immunoprecipitation,Western blot and Human,Mouse,Rat
Overview
Product Description | Rabbit Polyclonal antibody recognizes GLDC |
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Tested Reactivity | Hu, Ms, Rat |
Tested Application | ICC/IF, IP, WB |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | GLDC |
Antigen Species | Human |
Immunogen | Recombinant fusion protein corresponding to aa. 36-290 of Human GLDC (NP_000161.2). |
Conjugation | Un-conjugated |
Alternate Names | GCE; GCSP; HYGN1; Glycine dehydrogenase (decarboxylating), mitochondrial; EC 1.4.4.2; Glycine cleavage system P protein; Glycine decarboxylase; Glycine dehydrogenase (aminomethyl-transferring) |
Application Instructions
Application Suggestion |
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Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. | ||||||||
Positive Control | DU145 | ||||||||
Observed Size | 113 kDa |
Properties
Form | Liquid |
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Purification | Affinity purified. |
Buffer | PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol. |
Preservative | 0.02% Sodium azide |
Stabilizer | 50% Glycerol |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links |
Swiss-port # P23378 Human Glycine dehydrogenase (decarboxylating), mitochondrial Swiss-port # Q91W43 Mouse Glycine dehydrogenase (decarboxylating), mitochondrial |
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Gene Symbol | GLDC |
Gene Full Name | glycine dehydrogenase (decarboxylating) |
Background | Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).[provided by RefSeq, Jan 2010] |
Function | The glycine cleavage system catalyzes the degradation of glycine. The P protein (GLDC) binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein (GCSH). [UniProt] |
Cellular Localization | Mitochondrion,. [UniProt] |
Calculated MW | 113 kDa |
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