AFG3L2 Antibody
Product Specifications
Background
This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders.
NCBI Gene ID
10939
Swiss Prot
Q9Y4W6
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 538-797 of human AFG3L2 (NP_006787.2) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Cell Cycle, Neuroscience, Signal Transduction
Purification
Affinity purification
Positive Control
LO2
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.
Calculated Molecular Weight
Observed: 89kDa
Fragment
IgG
Symbol
AFG3L2
Positive Control 2
293T
Positive Control 3
HeLa
Positive Control 4
Mouse brain
Positive Control 5
Mouse heart
Positive Control 6
Mouse kidney
NCBI Official Name
AFG3-like AAA ATPase 2
NCBI Organism
Homo sapiens
Other Product Names
AFG3L2, FLJ25993, SCA28, SPAX5
Tested Applications
WB, IHC, IF
Physical Properties
Liquid
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