HMGCL Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: HMGCL
Target Synonym: 3 hydroxy 3 methylglutaryl CoA lyase;3 hydroxy 3 methylglutaryl Coenzyme A lyase;3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase (hydroxymethylglutaricaciduria);3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase;3-hydroxy-3-methylglutarate-CoA lyase;HL;HMG CoA lyase;HMG CoA Lyase Deficiency;HMG-CoA lyase;HMGCL;HMGCL;Hydroxymethylglutaricaciduria;Hydroxymethylglutaryl CoA lyase;Hydroxymethylglutaryl CoA lyase mitochondrial;Hydroxymethylglutaryl-CoA lyase;Mitochondrial 3 hydroxy 3 methylglutaryl CoA lyase;mitochondrial;MS725;OTTHUMP00000044830
Research Areas: Cancer;Metabolism;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P35914
Accession:
Background: The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Concentration: 0.4 mg/mL
Immunogen: Recombinant protein of human HMGCL
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:500-1:2000;IHC 1:50-1:200
Calculated MW: 34kDa
ObservedMW:
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HMGCL Polyclonal Antibody
HMGCL Polyclonal Antibody
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: HMGCL
Target Synonym: 3 hydroxy 3 methylglutaryl CoA lyase;3 hydroxy 3 methylglutaryl Coenzyme A lyase;3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase (hydroxymethylglutaricaciduria);3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase;3-hydroxy-3-methylglutarate-CoA lyase;HL;HMG CoA lyase;HMG CoA Lyase Deficiency;HMG-CoA lyase;HMGCL;HMGCL;Hydroxymethylglutaricaciduria;Hydroxymethylglutaryl CoA lyase;Hydroxymethylglutaryl CoA lyase mitochondrial;Hydroxymethylglutaryl-CoA lyase;Mitochondrial 3 hydroxy 3 methylglutaryl CoA lyase;mitochondrial;MS725;OTTHUMP00000044830
Research Areas: Cancer;Metabolism;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P35914
Accession:
Background: The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Concentration: 0.4 mg/mL
Immunogen: Recombinant protein of human HMGCL
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:500-1:2000;IHC 1:50-1:200
Calculated MW: 34kDa
ObservedMW:
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Description
Size: 200μL
Storage: Store at -20℃ Valid for 12 months. Avoid freeze / thaw cycles.
Shipping: The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
Exp date: 12 months
Category ID_II: Primary Antibodies
Category ID_III: Polyclonal Antibodies
Abbreviation: HMGCL
Target Synonym: 3 hydroxy 3 methylglutaryl CoA lyase;3 hydroxy 3 methylglutaryl Coenzyme A lyase;3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase (hydroxymethylglutaricaciduria);3 hydroxymethyl 3 methylglutaryl Coenzyme A lyase;3-hydroxy-3-methylglutarate-CoA lyase;HL;HMG CoA lyase;HMG CoA Lyase Deficiency;HMG-CoA lyase;HMGCL;HMGCL;Hydroxymethylglutaricaciduria;Hydroxymethylglutaryl CoA lyase;Hydroxymethylglutaryl CoA lyase mitochondrial;Hydroxymethylglutaryl-CoA lyase;Mitochondrial 3 hydroxy 3 methylglutaryl CoA lyase;mitochondrial;MS725;OTTHUMP00000044830
Research Areas: Cancer;Metabolism;Signal Transduction
Conjugation: Unconjugated
Host: Rabbit
Species reactivity: Human;Mouse;Rat
Application: WB;IHC
Isotype: IgG
Clonality: Polyclonal
Clone NO.:
UNIProt ID: P35914
Accession:
Background: The protein encoded by this gene belongs to the HMG-CoA lyase family. It is a mitochondrial enzyme that catalyzes the final step of leucine degradation and plays a key role in ketone body formation. Mutations in this gene are associated with HMG-CoA lyase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Concentration: 0.4 mg/mL
Immunogen: Recombinant protein of human HMGCL
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Purification method: Affinity purification
Dilution: WB 1:500-1:2000;IHC 1:50-1:200
Calculated MW: 34kDa
ObservedMW:
