FH/Fumarase polyclonal, anti-human, mouse, rat
€295.00
In stock
SKU
K000479P
Catalog Number: K000479P
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB, IF
Request Manual
Questions? Contact us!
Size: 100 μl
Other size: 50 μl
Isotype: Rabbit IgG
Applications: WB, IF
Request Manual
Questions? Contact us!
Background:
Fumarase (FH) is an enzyme that catalyzes the reversible hydration/dehydration of fumarate to malate in the mitochondria. Fumarase deficiency is caused by a mutation in the fumarase gene in humans. Fumarase deficiency is one of the few known deficiencies of the Krebs cycle or tricarboxylic acid cycle, the main enzymatic pathway of cellular aerobic respiration.
Synonyms: FMRD, HLRCC, LRCC, MCL, MCUL1
Cellular Location: Cytoplasm Mitochondrion
Immunogen:
Recombinant Protein
Gene Symbol: FH/Fumarase
Gene ID: 2271
Swiss prot: P07954
Calculated MW: 50kDa
Recommended dilution:
WB 1:1000-2000, IHC 1:100-200
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
Fumarase (FH) is an enzyme that catalyzes the reversible hydration/dehydration of fumarate to malate in the mitochondria. Fumarase deficiency is caused by a mutation in the fumarase gene in humans. Fumarase deficiency is one of the few known deficiencies of the Krebs cycle or tricarboxylic acid cycle, the main enzymatic pathway of cellular aerobic respiration.
Synonyms: FMRD, HLRCC, LRCC, MCL, MCUL1
Cellular Location: Cytoplasm Mitochondrion
Immunogen:
Recombinant Protein
Gene Symbol: FH/Fumarase
Gene ID: 2271
Swiss prot: P07954
Calculated MW: 50kDa
Recommended dilution:
WB 1:1000-2000, IHC 1:100-200
Purity:
Affinity purification
Storage Buffer:
Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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