Home  >  Products  >  DSS1 (26S Proteasome Complex Subunit DSS1, Split Hand/Foot Malformation Type 1 Protein, Deleted In Split Hand/Split Foot Protein 1, Split Hand/Foot Deleted Protein 1, SHFM1, SHFDG1)
DSS1 (26S Proteasome Complex Subunit DSS1, Split Hand/Foot Malformation Type 1 Protein, Deleted In Split Hand/Split Foot Protein 1, Split Hand/Foot Deleted Protein 1, SHFM1, SHFDG1)

DSS1 (26S Proteasome Complex Subunit DSS1, Split Hand/Foot Malformation Type 1 Protein, Deleted In Split Hand/Split Foot Protein 1, Split Hand/Foot Deleted Protein 1, SHFM1, SHFDG1)

Cat no: D9642-01D

Supplier: United States Biological
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The gene for DSS1 has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. DSS1 has been proposed to be a candidate 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. Applications: Suitable for use in ELISA and Immunohistochemistry. Other applications not tested. Recommended Dilution: ELISA: 1:1000 Immunohistochemistry (Formalin fixed paraffin embedded): 10ug/ml Optimal dilutions to be determined by the researcher. Storage and Stability: May be stored at 4 degrees C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degrees C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Catalogue number: D9642-01D
Reactivities: Human
Hosts: Rabbit
Applications: ELISA, Immunohistochemistry
Size: 50ug
Form: Supplied as a liquid in PBS, 0.1% sodium azide.
P type: Pab
Purity: Purified by Protein G affinity chromatography.
Additional info: Recognizes human SHFM1.

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