26S Proteasome Complex Subunit SEM1 (SEM1) Antibody
637€ (100 µl)
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935106861
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name
26S Proteasome Complex Subunit SEM1 (SEM1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx115811
tested applications
ELISA, WB, IF/ICC
Description
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.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | 26S Proteasome Complex Subunit SEM1 (SEM1) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Antigen Affinity Chromatography. |
| Size 1 | 100 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB, IF/ICC |
| Buffer | PBS, pH 7.3, containing 0.02% Sodium Azide and 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 | P60896 |
| Gene ID | 7979 |
| NCBI Accession | NP_006295.1 |
| OMIM | 601285 |
| Background | Antibody anti-SEM1 |
| Status | RUO |
Descripción
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26S Proteasome Complex Subunit SEM1 (SEM1) Antibody
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.
Ver Producto