Split Hand/foot Malformation (Ectrodactyly) Type 1 Proteins (SHFM1)

The product of SHFM1 has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. Additionally we are shipping SHFM1 Antibodies (41) and SHFM1 Kits (3) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
Rat SHFM1 SHFM1 680532  
SHFM1 7979 P60896
SHFM1 20422 P60897
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Top SHFM1 Proteins at antibodies-online.com

Showing 5 out of 5 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 30 to 35 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 30 to 35 Days
$4,331.68
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 11 to 12 Days
$405.71
Details
Yeast Cow His tag   1 mg Log in to see 60 to 71 Days
$2,082.67
Details
HOST_Escherichia coli (E. coli) Human Un-conjugated   50 μg Log in to see 2 to 3 Days
$498.21
Details

SHFM1 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
,
Mouse (Murine)

More Proteins for Split Hand/foot Malformation (Ectrodactyly) Type 1 (SHFM1) Interaction Partners

Human Split Hand/foot Malformation (Ectrodactyly) Type 1 (SHFM1) interaction partners

  1. Promoter methylation plays a role in modulating DSS1 gene expression. Promoter hypomethylation is a frequent event in melanoma and squamous cell carcinoma and is closely linked to poor prognosis.

  2. DSS1 is a multifunctional and intrinsically disordered protein. (Review)

  3. three phenotypic subregions within the SHFM1 locus link both size and genomic position of the chromosomal aberrations to the clinical variability seen in SHFM1 patients

  4. SHFM1 confers cell cycle progression and resistance to p53 (show TP53 Proteins) stabilizing drugs in gastric cancer cells.

  5. by targeting RPA (show RPA1 Proteins) and mimicking DNA, DSS1 functions with BRCA2 (show BRCA2 Proteins) in a two-component homologous recombination mediator complex in genome maintenance and tumor suppression

  6. Breast cancers with high DSS1 expression have worse prognosis and shorter relapse-free survival times.

  7. Mutation screening of the SHFM1 gene in familial breast/ovarian cancer cases.

  8. DSS1 protein is critically involved in the maintenance of the transformed phenotype in cervical cancer cells, and that it might be a specific, robust and reliable marker for early detection, diagnosis and trea (show TREH Proteins)

  9. DSS1 has a role in homologous recombinational repair in human cells

  10. p63 (show RPE65 Proteins) binds to an enhancer element in the SHFM1 locus and this element controls expression of DLX6 and DLX5 (show DLX5 Proteins) which are important for limb development.

Mouse (Murine) Split Hand/foot Malformation (Ectrodactyly) Type 1 (SHFM1) interaction partners

  1. 3.1 angstrom crystal structure of approximately 90-kilodalton BRCA2 domain bound to DSS1, which reveals three oligonucleotide-binding (OB) folds and a helix-turn-helix (HTH) motif

SHFM1 Protein Profile

Protein Summary

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.

Gene names and symbols associated with SHFM1

  • split hand/foot malformation (ectrodactyly) type 1 (Shfm1)
  • split hand/foot malformation (ectrodactyly) type 1 (SHFM1)
  • DSS1 protein
  • ECD protein
  • SEM1 protein
  • SHFD1 protein
  • Shfdg1 protein
  • Shfg protein
  • SHSF1 protein

Protein level used designations for SHFM1

26S proteasome complex subunit DSS1 , candidate for split hand/foot malformation type 1 , split hand/foot malformation (ectrodactyly) type 1 , 26 proteasome complex subunit DSS1 , split hand/foot malformation type 1 protein homolog , deleted in split hand/split foot protein 1 , deleted in split-hand/split-foot 1 , split hand/foot deleted protein 1 , split hand/foot malformation type 1 protein , deleted in split hand/split foot protein 1 homolog , split hand/foot deleted gene 1 , split hand/foot deleted protein 1 homolog

GENE ID SPECIES
680532 Rattus norvegicus
698349 Macaca mulatta
747549 Pan troglodytes
772237 Gallus gallus
100038817 Taeniopygia guttata
767981 Bos taurus
7979 Homo sapiens
20422 Mus musculus
608719 Canis lupus familiaris
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