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Rabbit Anti-LHFPL5/AF555 Conjugated antibody
Rabbit Anti-LHFPL5/AF555 Conjugated antibody
Lhfpl5; LHPL5_HUMAN; Lipoma HMGIC fusion partner like 5; Lipoma HMGIC fusion partner-like 5 protein.
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  • NO.:SL18242R-AF555
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Cow,Horse,Sheep,)
    Applications:ICC IF
    concentration:1mg/ml
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Details

Product Name Anti-LHFPL5/AF555
Chinese Name AF555标记的脂肪瘤高迁移率融合蛋白样蛋白5抗体
Alias Lhfpl5; LHPL5_HUMAN; Lipoma HMGIC fusion partner like 5; Lipoma HMGIC fusion partner-like 5 protein.  
Research Area Cell biology  immunology  Neurobiology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Cow, Horse, Sheep, )
Applications ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 24kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human LHFPL5
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
Storage Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Product Detail 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. [provided by RefSeq, Jul 2008]

Function:
May function in hair bundle morphogenesis.

Subcellular Location:
Membrane.

DISEASE:
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.

Similarity:
Belongs to the LHFP family.

Database links:

Entrez Gene: 222662 Human

Entrez Gene: 328789 Mouse

Entrez Gene: 294303 Rat

Omim: 609427 Human

SwissProt: Q8TAF8 Human

SwissProt: Q4KL25 Mouse

SwissProt: Q5PPI7 Rat

Unigene: 367947 Human

Unigene: 284760 Mouse

Unigene: 161732 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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