Gene: BHLHA9
Official Full Name: basic helix-loop-helix family member a9provided by HGNC
Gene Summary: 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). [provided by RefSeq, Mar 2015]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA02071 | BHLHA9 Knockout cell line (AC16) | Human | BHLHA9 | 1:3-1:4 | negative | Online Inquiry |
| KOA17513 | BHLHA9 Knockout cell line (BEAS-2B) | Human | BHLHA9 | 1:3~1:4 | negative | Online Inquiry |
| KOA32962 | BHLHA9 Knockout cell line (U-2932) | Human | BHLHA9 | 1:2-1:4 | negative | Online Inquiry |
| KOA48372 | BHLHA9 Knockout cell line (TPC-1) | Human | BHLHA9 | 1:5-1:8 | negative | Online Inquiry |
| KOA63772 | BHLHA9 Knockout cell line (NCM460) | Human | BHLHA9 | 1:2~1:3 | negative | Online Inquiry |
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