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BCL7B Polyclonal Antibody, 50ul Cell Screening and Imaging and may regulate imprinting in

SKU: 28079624408

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SEK162.00 SEK200.00

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BCL7B Polyclonal Antibody, 50ul Cell Screening and Imaging and may regulate imprinting inThis 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

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Description

and may regulate imprinting in this region

The encoded protein contains two chromodomains

The protein encoded by this gene contains WD-40 domains| in addition to an F-box motif| so it belongs to the Fbw class

|disease:Defects in CFD are the cause of complement factor D deficiency

The encoded protein may play a role in regulating vasculogenesis

BCL7B Polyclonal Antibody, 50ul Cell Screening and Imaging and may regulate imprinting inThis 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

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