26S Proteasome Complex Subunit SEM1 (SEM1) Protein
234€ (2 µg)
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name
26S Proteasome Complex Subunit SEM1 (SEM1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx262720
tested applications
SDS-PAGE
Description
SHFM1 is a recombinant protein. 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.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Proteins and Peptides |
| Immunogen Target | 26S Proteasome Complex Subunit SEM1 (SEM1) |
| Conjugation | Unconjugated |
| Expression | Recombinant |
| Purity | > 85% (SDS-PAGE) |
| Size 1 | 2 µg |
| Size 2 | 10 µg |
| Size 3 | 1 mg |
| Form | Liquid |
| Tested Applications | SDS-PAGE |
| Availability | Shipped within 5-10 working days. |
| Dry Ice | No |
| UniProt ID | P60896 |
| Gene ID | 7979 |
| NCBI Accession | NP_006295.1 |
| OMIM | 601285 |
| Background | Protein SEM1 |
| Status | RUO |
| Note | This product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use. |
Descripción
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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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