Family with Sequence Similarity 58, Member B 产品
(Family with Sequence Similarity 58, Member B (FAM58B))
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Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008].
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Family with Sequence Similarity 58, Member B 抗体
High quality antibodies with extensive validation data.
Recommended Family with Sequence Similarity 58, Member B 抗体
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
ELISA, IHC, WB
Validations
Cat. No.
ABIN4889081
Quantity
100 μg
Datasheet
Datasheet
Recommended Family with Sequence Similarity 58, Member B 蛋白
Synonyms and alternative names related to Family with Sequence Similarity 58, Member B
family with sequence similarity 58, member B (Fam58b), cyclin-related protein FAM58B (FAM58BP), 1810009O10Rik, Fam58a, FAM58B, RGD1305651Protein level used designations for Family with Sequence Similarity 58, Member B
- cyclin M
- cyclin-related protein FAM58A
- cyclin-related protein FAM58B
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- FAM9C
- FAM9B
- FAM9A
- FAM98C
- FAM98B
- FAM98A
- FAM96B
- FAM96A
- FAM92B
- FAM91A1
- FAM90A9P
- Fam90a9
- FAM90A8P
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