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 |