Serine Hydroxymethyltransferase, Mitochondrial (SHMT2) Antibody
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Description
Serine Hydroxymethyltransferase, Mitochondrial (SHMT2) Antibody is a Rabbit polyclonal antibody for the detection of Human Serine Hydroxymethyltransferase, Mitochondrial (SHMT2).
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Serine Hydroxymethyltransferase, Mitochondrial (SHMT2) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Size 1 | 50 µg |
| Size 2 | 100 µg |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC |
| Buffer | 0.01 M PBS, pH 7.4, 50% glycerol, 0.05% Proclin-300. |
| Availability | Shipped within 5-12 working days. |
| Storage | Store at 2-8 °C for up to 2 weeks. For long-term storage, aliquot and store at -80 °C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | P34897 |
| Gene ID | 6472 |
| NCBI Accession | NP_001159828.1 |
| Background | Antibody anti-SHMT2 |
| Status | RUO |
Descripción
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This gene encodes the mitochondrial form of a pyridoxal phosphate-dependent enzyme that catalyzes the reversible reaction of serine and tetrahydrofolate to glycine and 5, 10-methylene tetrahydrofolate. The encoded product is primarily responsible for glycine synthesis. The activity of the encoded protein has been suggested to be the primary source of intracellular glycine. The gene which encodes the cytosolic form of this enzyme is located on chromosome 17. Alternative splicing results in multiple transcript variants.
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Serine Hydroxymethyltransferase, Mitochondrial (SHMT2) Antibody
SHMT2 Antibody is a Rabbit Polyclonal antibody against SHMT2. This gene encodes the mitochondrial form of a pyridoxal phosphate-dependent enzyme that catalyzes the reversible reaction of serine and tetrahydrofolate to glycine and 5,10-methylene tetrahydrofolate. The encoded product is primarily responsible for glycine synthesis. The activity of the encoded protein has been suggested to be the primary source of intracellular glycine. The gene which encodes the cytosolic form of this enzyme is located on chromosome 17. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009].
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