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SLC25A12 antibody
Slc25a12
Reactivity: Human, Mouse
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-SLC25A12 Antibody
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Target
See all SLC25A12 (Slc25a12) Antibodies
SLC25A12 (Slc25a12)
(Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12))
Reactivity
All reactivities for SLC25A12 antibodies
Human, Mouse
Host
All hosts for SLC25A12 antibodies
Rabbit
Clonality
All clonalities for SLC25A12 antibodies
Polyclonal
Conjugate
All conjugates for SLC25A12 antibodies
This SLC25A12 antibody is un-conjugated
Application
All applications for SLC25A12 antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Synthetic peptide of human SLC25A12
Isotype
IgG
Top Product
Discover our top product Slc25a12 Primary Antibody
Alternatives
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anti-Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12) (Middle Region) antibody
Slc25a12
Reactivity: Human, Mouse, Rat, Cow, Dog, Pig, Rabbit, Guinea Pig, Horse
WB, IHC
Host: Rabbit
Polyclonal
unconjugated
anti-Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12) (C-Term) antibody
Slc25a12
Reactivity: Human, Mouse, Rat, Monkey, Cow, Dog, Pig, Rabbit, Bat
WB
Host: Rabbit
Polyclonal
unconjugated
Application Details
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Application Notes
IHC 1:25-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.4 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for SLC25A12
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Target
SLC25A12 (Slc25a12)
(Solute Carrier Family 25 (Mitochondrial Carrier, Aralar), Member 12 (Slc25a12))
Alternative Name
SLC25A12 (Slc25a12 Products )
Background
This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene.
NCBI Accession
NP_003696
UniProt
O75746
Pathways
Ribonucleoside Biosynthetic Process , Dicarboxylic Acid Transport
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