LHFPL5 antibody (C-Term)

Catalog No. ABIN5539148

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)

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.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

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: 24 kDa

Gene ID: 222662

UniProt: Q8TAF8

Pathways: Sensory Perception of Sound