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BCL7B encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. Zusätzlich bieten wir Ihnen B-Cell CLL/lymphoma 7B Proteine (9) und und viele weitere Produktgruppen zu diesem Protein an.
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We herewith propose that the BCL7B gene, located in the chromosomal region commonly deleted in Williams syndrome, could potentially have a role in this particular association.
our data indicate that BCL7B/BCL-7 has some roles in maintaining the structure of nuclei and is involved in the modulation of multiple pathways, including Wnt and apoptosis.
BCL7B gene deltion is associated with Williams-Beuren Syndrome leading to Burkitt Leukemia.
This gene encodes a member of the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment of BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene.
B-cell CLL/lymphoma 7 protein family member B-B
, B-cell CLL/lymphoma 7 protein family member B
, B-cell CLL/lymphoma 7 protein family member B-A
, B-cell CLL/lymphoma 7B
, B-cell CLL/lymphoma 7b