28S rRNA (Cytosine-C(5))-Methyltransferase (NSUN5) Antibody
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Description
28S rRNA (Cytosine-C(5))-Methyltransferase (NSUN5) Antibody is a Rabbit Polyclonal antibody against NSUN5. This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.
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Product specifications
| Category | Primary Antibodies |
| Immunogen Target | 28S rRNA (Cytosine-C(5))-Methyltransferase (NSUN5) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/1000, IHC-P: 1/50 - 1/200. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified by affinity chromatography. |
| Size 1 | 20 µl |
| Size 2 | 100 µl |
| Size 3 | 2 × 100 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC |
| Buffer | PBS, pH 7.3, containing 0.01% thimerosal, 50% glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q96P11 |
| Gene ID | 55695 |
| NCBI Accession | NP_060514.1 |
| Background | Antibody anti-NSUN5 |
| Status | RUO |
| Note | Concentration: > 0.2 mg/ml - |
Descripción
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28S rRNA (Cytosine-C(5))-Methyltransferase (NSUN5) Antibody
28S rRNA (Cytosine-C(5))-Methyltransferase (NSUN5) Antibody is a Rabbit Polyclonal antibody against NSUN5. This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.
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