PJVK Antibody
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) .
NCBI Gene ID
494513
Swiss Prot
Q0ZLH3
Accession Number
Q0ZLH3
Host
Rabbit
Reactivity
Human
Immunogen
This PJVK antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 170-197 amino acids from the Central region of human PJVK.
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Neuroscience
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Concentration
Batch dependent
Buffer
Supplied in PBS with 0.09% (W/V) sodium azide.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
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.
Calculated Molecular Weight
40 kDa
Fragment
Rabbit Ig
Applications Notes
For WB starting dilution is: 1:1000
Symbol
DFNB59
NCBI Official Name
Pejvakin
NCBI Organism
Homo sapiens
Background Reference 01
Mahdieh, N., et al. J. Hum. Genet. 55 (10) :639-648 (2010)
Background Reference 02
Bailey, S.D., et al. Diabetes Care 33 (10) :2250-2253 (2010)
Background Reference 03
Talmud, P.J., et al. Am. J. Hum. Genet. 85 (5) :628-642 (2009)
Background Reference 04
Hashemzadeh Chaleshtori, M., et al. Clin. Genet. 72 (3) :261-263 (2007)
Other Product Names
Pejvakin, Autosomal recessive deafness type 59 protein, DFNB59, PJVK
Tested Applications
WB
Protein ID
114152117
Physical Properties
Liquid
Curated Selection
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