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Anti-ALAD Polyclonal Antibody
Catalog No. TMAB-02424 Copy Product Info
🥰Excellent
Anti-ALAD Polyclonal Antibody is a Rabbit antibody targeting ALAD. Anti-ALAD Polyclonal Antibody can be used in WB.
Anti-ALAD Polyclonal Antibody
Copy Product Info🥰Excellent
Catalog No. TMAB-02424
Anti-ALAD Polyclonal Antibody is a Rabbit antibody targeting ALAD. Anti-ALAD Polyclonal Antibody can be used in WB.
Anti-ALAD Polyclonal Antibody
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 50 μL | $221 | 7-10 days | 7-10 days | |
| 100 μL | $372 | 7-10 days | 7-10 days | |
| 200 μL | $527 | 7-10 days | 7-10 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
Antigen Details
Chemical Properties
Stability & Storage
| Description | Anti-ALAD Polyclonal Antibody is a Rabbit antibody targeting ALAD. Anti-ALAD Polyclonal Antibody can be used in WB. |
| Ig Type | IgG |
| Reactivity | Mouse (predicted:Rat,Cow,Sheep,Dog,Rabbit,Horse,Human) |
| Verified Activity | 25 μg total protein per lane of various lysates (see on figure) probed with ALAD polyclonal antibody, unconjugated (TMAB-02424) at 1:1000 dilution and 4°C overnight incubation. Followed by conjugated secondary antibody incubation at r. T. for 60 min. |
| Application | |
| Recommended Dose | WB: 1:500-2000 |
| Antibody Type | Polyclonal |
| Host Species | Rabbit |
| Construction | Polyclonal Antibody |
| Purification | Protein A purified |
| Appearance | Liquid |
| Formulation | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| Concentration | 1mg/ml |
| Research Background | Catalyzes an early step in the biosynthesis of tetrapyrroles. Binds two molecules of 5-aminolevulinate per subunit, each at a distinct site, and catalyzes their condensation to form porphobilinogen. Involvement in disease:Defects in ALAD are the cause of acute hepatic porphyria (AHP). AHP is a form of porphyria. Porphyrias are inherited defects in the biosynthesis of heme, resulting in the accumulation and increased excretion of porphyrins or porphyrin precursors. They are classified as erythropoietic or hepatic, depending on whether the enzyme deficiency occurs in red blood cells or in the liver. AHP is characterized by attacks of gastrointestinal disturbances, abdominal colic, paralysis, and peripheral neuropathy. Most attacks are precipitated by drugs, alcohol, caloric deprivation, infections, or endocrine factors. |
| Immunogen | KLH conjugated synthetic peptide: human ALAD |
| Antigen Species | Human |
| Gene Name | ALAD |
| Gene ID | |
| Protein Name | delta-aminolevulinic acid dehydratase |
| Uniprot ID | |
| Function | Catalyzes an early step in the biosynthesis of tetrapyrroles. Binds two molecules of 5-aminolevulinate per subunit, each at a distinct site, and catalyzes their condensation to form porphobilinogen. |
| Molecular Weight | Theoretical: 36 kDa. Actual: 36 kDa. |
| Stability & Storage | Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
| Transport | Shipping with blue ice. |
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