Human HMGCL (Hydroxymethylglutaryl-Coa Lyase, Mitochondrial) - Recombinant Protein
Beta LifeScience
SKU/CAT #: BLT-01389P

SDS-PAGE analysis of Human HMGCL (Hydroxymethylglutaryl-Coa Lyase, Mitochondrial) - Recombinant Protein, CAT# BLT-01389P, showing >90% purity under 15% SDS-PAGE (Reduced)
Human HMGCL (Hydroxymethylglutaryl-Coa Lyase, Mitochondrial) - Recombinant Protein
Beta LifeScience
SKU/CAT #: BLT-01389P
Regular price
$59500
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Quantity Pricing
Pack Size | Price (USD) |
---|---|
500 µg | $1,030 (Fall Promotion) |
1 mg | $1,870 (Fall Promotion) |
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Product Overview
Product Name | Recombinant Human 3-Hydroxymethyl-3-Methylglutaryl Coenzyme A Lyase (HMGCL) Protein |
Product Overview | This recombinant human 3-Hydroxymethyl-3-Methylglutaryl Coenzyme A Lyase (HMGCL) protein includes amino acids 1-325aa of the target gene is expressed in E.coli.The protein is supplied in lyophilized form and formulated in phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5% trehaloseprior to lyophilization. |
Target Uniprot Id | P35914 |
Recommended Name | Hydroxymethylglutaryl-CoA lyase, mitochondrial |
Gene Name | HMGCL |
Synonyms | Hydroxymethylglutaryl-CoA lyase, HL |
Species | Human |
Predicted Molecular Mass | 38 kDa |
Expression System | E.coli |
Expression Range | 1-325aa |
Tag | N-6His |
Purity | >90% |
Formulation | Lyophilized |
Buffer | Phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5%Trehalose |
Storage Condition | 1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C. |
Reconstitution Instruction | Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%. |
Applications | Positive Control; Immunogen; SDS-PAGE; WB |
Research Area | Signal Transduction |
Target Function | Mitochondrial 3-hydroxymethyl-3-methylglutaryl-CoA lyase that catalyzes a cation-dependent cleavage of (S)-3-hydroxy-3-methylglutaryl-CoA into acetyl-CoA and acetoacetate, a key step in ketogenesis. Terminal step in leucine catabolism. Ketone bodies (beta-hydroxybutyrate, acetoacetate and acetone) are essential as an alternative source of energy to glucose, as lipid precursors and as regulators of metabolism. |
Subcellular Location | Mitochondrion matrix. Peroxisome. |
Protein Family | HMG-CoA lyase family |
Associated Diseases | 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (HMGCLD) |
Tissue Specificity | Highest expression in liver. Expressed in pancreas, kidney, intestine, testis, fibroblasts and lymphoblasts. Very low expression in brain and skeletal muscle. The relative expression of isoform 2 (at mRNA level) is highest in heart (30%), skeletal muscle |