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ZN883 Rabbit Polyclonal Antibody, 100ul Peptide Modification This gene is deleted in
ZN883 Rabbit Polyclonal Antibody, 100ul Peptide Modification This gene is deleted in
ZN883 Rabbit Polyclonal Antibody, 100ul Peptide Modification This gene is deleted in
ZN883 Rabbit Polyclonal Antibody, 100ul Peptide Modification This gene is deleted in

ZN883 Rabbit Polyclonal Antibody, 100ul Peptide Modification This gene is deleted in

SKU: 93752906511

4.2
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ZN883 Rabbit Polyclonal Antibody, 100ul Peptide Modification This gene is deleted in

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Description

This gene is deleted in Williams syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11

miscellaneous:5 FOXD4-like proteins (FOXD4L2

This protein is chemotactic in vitro for thymocytes and activated T cells| but not for B cells| macrophages| or neutrophils

This protein mediates the interaction of C8 with the C5b-7 membrane attack complex precursor

The transcript produced from this gene has an unusually large 3' UTR which has not been completely sequenced

ZN883 Rabbit Polyclonal Antibody, 100ul Peptide Modification This gene is deleted in

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