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KBTBD10


Official Full Name
kelch like family member 41
Organism
Homo sapiens
Gene ID
10324
Background
This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder. [provided by RefSeq, Mar 2015]
Synonyms
KLHL41; Krp1; KBTBD10; SARCOSIN

Cat.No. Product Name Price
SHH322551 shRNA set against Mouse KBTBD10 (NM_001081087.1) Inquiry
SHH322555 shRNA set against Rat KBTBD10 (NM_057191.1) Inquiry
SHL187598 shRNA set against Rat Kbtbd10(NM_057191.1) Inquiry
SHL187604 shRNA set against Mouse Kbtbd10(NM_001081087.1) Inquiry
SHL187704 shRNA set against Human KBTBD10(NM_006063.2) Inquiry
Cat.No. Product Name Price
CDFH009580 Human KBTBD10 cDNA Clone(NM_006063.2) Inquiry
CDFH009581 Human KBTBD10 cDNA Clone(NM_006063.2) Inquiry
CDFR013769 Rat Kbtbd10 cDNA Clone(NM_057191.1) Inquiry
MiUTR1H-05087 KBTBD10 miRNA 3'UTR clone Inquiry
MiUTR1M-06197 KBTBD10 miRNA 3'UTR clone Inquiry
MiUTR1R-02784 KBTBD10 miRNA 3'UTR clone Inquiry
CDCL122681 Human Kbtbd10 ORF clone (NM_001081087.1) Inquiry
CDCR291928 Human KBTBD10 ORF Clone(NM_006063.2) Inquiry
CDCR380802 Rat Kbtbd10 ORF Clone(NM_057191.1) Inquiry
CDCS412543 Human KBTBD10 ORF Clone (BC006534) Inquiry
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