PJVK rabbit pAb
The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). [provided by RefSeq, Dec 2008],
Product Specifications
Background
The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59) . [provided by RefSeq, Dec 2008]
Product Name Alternative
Pejvakin (Autosomal recessive deafness type 59 protein)
UniProt
Q0ZLH3
Swiss Prot
Q0ZLH3
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human PJVK AA range: 69-119
Target
PJVK
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Molecular Weight
38kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
38kD
Fragment
IgG
Subcellular Location
Peroxisome membrane . Cell projection, cilium . Associates with the peroxisomal membrane; it is unclear whether it is embedded or just associated with the peroxisomal membrane. Localizes to ciliary rootlet. .
Other Product Names
Pejvakin (Autosomal recessive deafness type 59 protein)
Gene ID (Human)
494513
Available Sizes
Curated Selection
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