中文名称:兔抗BHLHA9多克隆抗体
| Background: | This gene is a member of the basic helix-loop-helix family. The encoded protein is a transcription factor involved in limb development. Mutations in this gene have been associated with mesoaxial synostotic syndactyly Malik-Percin type (MSSD). Copy number variation of a locus containing this gene has been linked to a form of split-hand/foot malformation with long bone deficiency (SHFLD3). | 
| Applications: | ELISA, WB | 
| Name of antibody: | BHLHA9 | 
| Immunogen: | Synthetic peptide of human BHLHA9 | 
| Full name: | basic helix-loop-helix family member a9 | 
| Synonyms: | BHLHF42 | 
| SwissProt: | Q7RTU4 | 
| ELISA Recommended dilution: | 5000-10000 | 
| WB Predicted band size: | 24 kDa | 
| WB Positive control: | Human cerebrum tissue lysate | 
| WB Recommended dilution: | 200-1000 | 
	
 
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