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Pejvakin antibody (AA 170-197)
This Rabbit Polyclonal antibody specifically detects Pejvakin in WB. It exhibits reactivity toward Human.
Catalog No. ABIN1537942
$383.35
$451.00
save $67.65 (-15 %)
Plus shipping costs $50.00
80 μL ABIN2849566
400 μL ABIN1537942
80 μL ABIN2849566
400 μL ABIN1537942
Delivery in 10 to 11 Business Days
Quick Overview for Pejvakin antibody (AA 170-197) (ABIN1537942)
Target
See all Pejvakin (DFNB59) Antibodies
Pejvakin (DFNB59)
(Deafness, Autosomal Recessive 59 (DFNB59))
Reactivity
Human
Host
All hosts for Pejvakin antibodies
Rabbit
Clonality
All clonalities for Pejvakin antibodies
Polyclonal
Conjugate
All conjugates for Pejvakin antibodies
This Pejvakin antibody is un-conjugated
Application
All applications for Pejvakin antibodies
Western Blotting (WB)
Clone
RB37747
Product Details anti-Pejvakin Antibody
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Binding Specificity
All epitopes for Pejvakin antibodies
AA 170-197
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
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.
Isotype
Ig Fraction
Alternatives
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Application Details
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Application Notes
WB: 1:1000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
PJVK Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
Expiry Date
6 months
Target Details for Pejvakin
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Target
Pejvakin (DFNB59)
(Deafness, Autosomal Recessive 59 (DFNB59))
Alternative Name
PJVK
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).
Molecular Weight
39913
Gene ID
494513
NCBI Accession
NP_001036167
UniProt
Q0ZLH3
Pathways
Sensory Perception of Sound
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