LHFPL5 antibody (C-Term)

Catalog No. ABIN654373

Product Details anti-LHFPL5 Antibody

Target: LHFPL5 (Lipoma HMGIC Fusion Partner-Like 5 (LHFPL5))

Binding Specificity: AA 186-214, C-Term

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This LHFPL5 antibody is un-conjugated

Application: Western Blotting (WB)

Predicted Reactivity: Rat

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This LHFPL5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 186-214 amino acids from the C-terminal region of human LHFPL5.

Clone: RB28242

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

Target Details for LHFPL5

Target: LHFPL5 (Lipoma HMGIC Fusion Partner-Like 5 (LHFPL5))

Alternative Name: LHFPL5 (LHFPL5 Products)

Synonyms: DFNB67 antibody, TMHS antibody, dJ510O8.8 antibody, 9330179O15Rik antibody, Tmhs antibody, hscy antibody, PMP22A antibody, lhfpl5 antibody, zgc:171589 antibody, LHFPL tetraspan subfamily member 5 antibody, lipoma HMGIC fusion partner-like 5 antibody, LHFPL tetraspan subfamily member 5b antibody, LHFPL5 antibody, Lhfpl5 antibody, lhfpl5b antibody

Background: This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis.

Molecular Weight: 24201

Gene ID: 222662

NCBI Accession: NP_872354

UniProt: Q8TAF8

Pathways: Sensory Perception of Sound