CLN3 Antibody
Product Specifications
Background
This gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs) . Many alternatively spliced transcript variants have been found for this gene.
NCBI Gene ID
1201
Swiss Prot
Q13286
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-280 of human CLN3 (NP_001035897.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Apoptosis, Cell Cycle, Neuroscience
Purification
Affinity purification
Positive Control
Mouse liver
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=18-394
Calculated Molecular Weight
Observed: 48kDa
Fragment
IgG
Symbol
CLN3
Positive Control 2
Rat liver
NCBI Official Name
CLN3 lysosomal/endosomal transmembrane protein, battenin
NCBI Organism
Homo sapiens
Other Product Names
BTN1, BTS, JNCL, battenin, CLN3, battenin, batten disease protein, ceroid-lipofuscinosis, neuronal 3
Tested Applications
WB, IHC
Physical Properties
Liquid
Curated Selection
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