LHFPL5 Antibodies

AND LHFPL5 ELISA kits, LHFPL5 Proteins

Many biological assays use antibodies to detect LHFPL5, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with LHFPL5 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop LHFPL5 antibodies...

We validate the specificity of these antibodies to LHFPL5 by testing them on tissues known to express LHFPL5 positively and negatively. Browse below to find the LHFPL5 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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LHFPL5 Infographic by Boster Bio

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LHFPL5 (NM_182548) Human Over-expression Lysate

Human

$628
Cat # LS222662
100 µg

LHFPL5 Overview

Facts about LHFPL tetraspan subfamily member 5 protein.

LHFPL5 3D structure. Source: alphafold

LHFPL tetraspan subfamily member 5 protein (LHFPL5)

In the inner ear, might be a part of the hair cell's mechanotransduction machines that functionally couples PCDH15 into the transduction channel. Regulates transducer channel conductance and is needed for fast channel adaptation (By similarity).

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Gene Information

Human
Gene Name:	LHFPL5
Uniprot:	Q8TAF8
Entrez:	222662

Family

Belongs to:

LHFP family

Alternative Names

LHFPL tetraspan subfamily member 5 protein

Molecular Weight

Mass (kDA):
24.201 kDA

Genomic Context


Human

Location:	6p21.31
Sequence:	6; NC_000006.12 (35805352..35824070)

Subcellular Localizations

Cell membrane; Multi-pass membrane protein. Efficient localization to the plasma membrane requires the presence of PCDH15.

Diseases

Deafness, autosomal recessive, 67 (DFNB67)

Interacting Proteins

CCDC155
GGT7
GPRC5D

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/LHFPL5

References

PMID: 16752389 by Kalay E., et al. Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss.

PMID: 16459341 by Shabbir M.I., et al. Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.