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Anti-HMGCL Polyclonal Antibody

Catalog No. TMAB-07186 Copy Product Info
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Anti-HMGCL Polyclonal Antibody is a Rabbit antibody targeting HMGCL. Anti-HMGCL Polyclonal Antibody can be used in WB.

Anti-HMGCL Polyclonal Antibody

Copy Product Info
🥰Excellent
Catalog No. TMAB-07186

Anti-HMGCL Polyclonal Antibody is a Rabbit antibody targeting HMGCL. Anti-HMGCL Polyclonal Antibody can be used in WB.

Anti-HMGCL Polyclonal Antibody
Pack SizePriceUSA StockGlobal StockQuantity
50 μL$2207-10 days7-10 days
100 μL$3717-10 days7-10 days
200 μL$5287-10 days7-10 days
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
Anti-HMGCL Polyclonal Antibody is a Rabbit antibody targeting HMGCL. Anti-HMGCL Polyclonal Antibody can be used in WB.
Ig Type
IgG
Reactivity
Mouse (predicted:Human,Rat,Chicken,Dog,Horse,Rabbit)
Verified Activity
Sample: Liver (Mouse) Lysate at 40 μg
Primary: Anti-HMGCL (TMAB-07186) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 32 kD
Observed band size: 30 kD
Application
Recommended Dose
WB: 1:500-2000
Antibody Type
Polyclonal
Host SpeciesRabbit
Subcellular LocalizationMitochondrion matrix.
Tissue SpecificityFibroblasts, liver and lymphoblasts.
ConstructionPolyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundHydroxymethylglutaryl-CoA lyase (HMGCL) is found in fibroblasts, liver and lymphoblasts. It has a role in ketogenesis and leucine catabolism. Defects in HMGCL are the cause of 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (hydroxymethylglutaricaciduria), an autosomal recessive disease which can lead to hypoglycemia and coma.
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human HMGCL
Antigen Species
Human
Gene Name
HMGCL
Gene ID
Protein Name
Hydroxymethylglutaryl-CoA lyase, mitochondrial
Uniprot ID
Function
Key enzyme in ketogenesis (ketone body formation). Terminal step in leucine catabolism.
Chemical Properties
Molecular WeightTheoretical: 32 kDa.
Stability & Storage
Stability & StorageStore at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
TransportShipping with blue ice.

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