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Recombinant LHFPL5 Monoclonal Antibody

Product Specifications

Background

Defects in LHFPL5 are a cause of deafness autosomal recessive type 67 (DFNB67) [MIM:610265]. DFNB67 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.

Abbreviation

LHFPL5

UniProt

Q8TAF8

Host

Rabbit

Reactivity

Human; Mouse; Rat

Immunogen

Recombinant Human LHFPL5 protein

Target

Lhfpl; TMHS; LHFPL5

Clonality

Monoclonal,Recombinant

Clone

4B9

Conjugation

Unconjugated

Applications

WB

Purification

Protein A

Concentration

0.2 mg/mL

Dilution

WB 1:1000-1:5000

Buffer

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Shipping Conditions

Ice bag

Storage Conditions

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

Product MSDS

https://789.bio/eb/65k5z9q8

Calculated Molecular Weight

24 kDa

Observed Molecular Weight

24 kDa

Isotype

IgG, κ

Available Sizes

Curated Selection

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