SBDS antibody
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935106861
info@markelab.com
name
SBDS antibody
category
Primary Antibodies
provider
FineTest
reference
FNab07617
tested applications
ELISA, WB, IHC, IF
Description
This gene encodes a highly conserved protein that plays an essential role in ribosome biogenesis. The encoded protein interacts with elongation factor-like GTPase 1 to disassociate eukaryotic initiation factor 6 from the late cytoplasmic pre-60S ribosomal subunit allowing assembly of the 80S subunit. Mutations within this gene are associated with the autosomal recessive disorder Shwachman-Bodian-Diamond syndrome. This gene has a closely linked pseudogene that is distally located.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Shwachman-Bodian-Diamond syndrome (SBDS) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IHC: 1:50 - 1:100; IF: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 34 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IHC, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.) |
| UniProt ID | Q9Y3A5 |
| Gene ID | 51119 |
| Alias | Ribosome maturation protein SBDS,Shwachman-Bodian-Diamond syndrome protein,SBDS |
| Background | Antibody anti-SBDS |
| Status | RUO |
| Note | Mol. Weight 34 kDa |
Descripción
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Human SBDS (Ribosome maturation protein SBDS) ELISA Kit
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SBDS antibody
This gene encodes a highly conserved protein that plays an essential role in ribosome biogenesis. The encoded protein interacts with elongation factor-like GTPase 1 to disassociate eukaryotic initiation factor 6 from the late cytoplasmic pre-60S ribosomal subunit allowing assembly of the 80S subunit. Mutations within this gene are associated with the autosomal recessive disorder Shwachman-Bodian-Diamond syndrome. This gene has a closely linked pseudogene that is distally located.
Ver Producto