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