S2546 rabbit pAb
This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016],
Product Specifications
Background
This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]
UniProt
Q96AG3
Swiss Prot
Q96AG3
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human S2546 AA range: 322-372
Target
S2546
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Mitochondrion outer membrane ; Multi-pass membrane protein .
Gene ID (Human)
91137
Available Sizes
Curated Selection
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items
![3- (4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl) -5- (trifluoromethyl) -1H-pyrrolo[2,3-b]pyridine](https://cdn.genprice.uk/genprice/uk/genprice4.webp)
sc-311961 250 mg
3- (4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl) -5- (trifluoromethyl) -1H-pyrrolo[2,3-b]pyridine
Ask
View Details 
