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B9D1
B9 domain containing 1B9, EPPB9, MKS9, MKSR-1
This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]
Top validated antibodies |
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| LSBio |  LS-C409517 |
Polyclonal |
WB
IHC
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| antibodies-online | ABIN1450121 |
1 references | Polyclonal |
WB
EL
ICC
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| Invitrogen Antibodies | PA5-96883 |
Polyclonal |
WB
EL
ICC
IHC
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| GeneTex | GTX32055 |
Polyclonal |
WB
EL
ICC
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| Boster Biological Technology | A10722 |
Polyclonal |
WB
EL
ICC
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