SEM1 antibody
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935106861
info@markelab.com
name
SEM1 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab02547
tested applications
ELISA, WB, IHC, IF
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | split hand/foot malformation(ectrodactyly) type 1 (SEM1) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | WB: 1:200-1:2000; IHC: 1:50-1:500 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 8-10 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 | P60896 |
| Gene ID | 7979 |
| Alias | 26S proteasome complex subunit SEM1,26S proteasome complex subunit DSS1,Deleted in split hand/split foot protein 1,Split hand/foot deleted protein 1,Split hand/foot malformation type 1 protein,SEM1,C7orf76,DSS1,SHFDG1,SHFM1 |
| Background | Antibody anti-SEM1 |
| Status | RUO |
| Note | Mol. Weight 8-10 kDa |
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Split Hand/Foot Malformation (Ectrodactyly) Type 1 Antibody is a Rabbit Polyclonal antibody against Split Hand/Foot Malformation (Ectrodactyly) Type 1. The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle.
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