Bhlha9 Antibodies

AND Bhlha9 ELISA kits, Bhlha9 Proteins

Many biological assays use antibodies to detect Bhlha9, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Bhlha9 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Bhlha9 antibodies...

We validate the specificity of these antibodies to Bhlha9 by testing them on tissues known to express Bhlha9 positively and negatively. Browse below to find the Bhlha9 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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Bhlha9 Infographic by Boster Bio

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Class A basic helix loop helix protein 9 (BHLHA9) (NM_001164405) Human Recombinant Protein

$1249
Cat # PROTQ7RTU4
20 µg

Bhlha9 Overview

Facts about Class A basic helix-loop-helix protein 9.

Class A basic helix-loop-helix protein 9 (Bhlha9)

Transcription factor, which play a role in limb development. Is an essential player in the regulatory system governing transcription of genes implicated in limb morphogenesis.

Gene Information

Mouse
Gene Name:	Bhlha9
Uniprot:	Q5RJB0
Entrez:	320522

Family

Belongs to:

No superfamily

Alternative Names

Basic Helix-Loop-Helix Family, Member A9; bHLHa9; BHLHF42; Class A Basic Helix-Loop-Helix Protein 9; Class F Basic Helix-Loop-Helix Factor 42; Class II Basic Helix-Loop-Helix Protein

Molecular Weight

Mass (kDA):
25.115 kDA

Genomic Context


Mouse

Location:	11\|11 B5
Sequence:	11;

Diseases

Limb Deformities, Congenital
Chromosomal Duplication
Developmental Delay (disorder)
Miller Dieker Syndrome
Ectrodactyly
Muscle Hypotonia
Congenital Disorders
Lissencephaly

Autistic Disorder
Congenital Hand Deformities

Pathways

Limb Development

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Bhlha9

References

PMID: 22147889 by Klopocki E., et al. Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion.