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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