Shopping Cart
Remove All
Your shopping cart is currently empty
Anti-beta glucuronidase Polyclonal Antibody
Catalog No. TMAB-03112 Copy Product Info
🥰Excellent
Anti-beta glucuronidase Polyclonal Antibody is a Rabbit antibody targeting beta glucuronidase. Anti-beta glucuronidase Polyclonal Antibody can be used in WB.
Anti-beta glucuronidase Polyclonal Antibody
Copy Product Info🥰Excellent
Catalog No. TMAB-03112
Anti-beta glucuronidase Polyclonal Antibody is a Rabbit antibody targeting beta glucuronidase. Anti-beta glucuronidase Polyclonal Antibody can be used in WB.
Anti-beta glucuronidase Polyclonal Antibody
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 50 μL | $221 | 7-10 days | 7-10 days | |
| 100 μL | $371 | 7-10 days | 7-10 days | |
| 200 μL | $529 | 7-10 days | 7-10 days |
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
Add to Cart
Add to Quotation
For research use only—not for human use. No sales to individuals. Use as intended only.
Resource Download
Product Introduction
Bioactivity
Antigen Details
Chemical Properties
Stability & Storage
| Description | Anti-beta glucuronidase Polyclonal Antibody is a Rabbit antibody targeting beta glucuronidase. Anti-beta glucuronidase Polyclonal Antibody can be used in WB. |
| Ig Type | IgG |
| Reactivity | Mouse (predicted:Human,Rat,Chicken,Dog,Pig,Cow) |
| Verified Activity | Sample: Intestine (Mouse) Lysate at 40 μg Primary: Anti-beta glucuronidase (TMAB-03112) at 1/300 dilution Secondary: HRP conjugated Goat-Anti-rabbit IgG at 1/5000 dilution Predicted band size: 69 kD Observed band size: 69 kD |
| Application | |
| Recommended Dose | WB: 1:500-2000 |
| Antibody Type | Polyclonal |
| Host Species | Rabbit |
| Subcellular Localization | Lysosome. |
| 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 | Defects in GUSB are the cause of mucopolysaccharidosis type 7 (MPS7) ; also known as Sly syndrome. MPS7 is an autosomal recessive lysosomal storage disease characterized by inability to degrade glucuronic acid-containing glycosaminoglycans. The phenotype is highly variable, ranging from severe lethal hydrops fetalis to mild forms with survival into adulthood. Most patients with the intermediate phenotype show hepatomegaly, skeletal anomalies, coarse facies, and variable degrees of mental impairment. Mucopolysaccharidosis type 7 is associated with non-immune hydrops fetalis, a generalized edema of the fetus with fluid accumulation in the body cavities due to non-immune causes. Non-immune hydrops fetalis is not a diagnosis in itself but a symptom, a feature of many genetic disorders, and the end-stage of a wide variety of disorders. |
| Immunogen | KLH conjugated synthetic peptide: human GUSB/beta glucuronidase |
| Antigen Species | Human |
| Gene Name | GUSB |
| Gene ID | |
| Protein Name | beta-glucuronidase |
| Uniprot ID | |
| Function | Plays an important role in the degradation of dermatan and keratan sulfates. |
| Molecular Weight | Theoretical: 69 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. |
Calculator
Preview
Related Tags: buy Anti-beta glucuronidase Polyclonal Antibody | purchase Anti-beta glucuronidase Polyclonal Antibody | Anti-beta glucuronidase Polyclonal Antibody cost | order Anti-beta glucuronidase Polyclonal Antibody | Anti-beta glucuronidase Polyclonal Antibody molecular weight
Generate Quote
Catalog No.: Cas No.:
Add
| Size | Quantity | Unit Price | Amount | Operation |
|---|
Generate Quote
- TOP
Feedback
Hello! How can I help you today? 
Copyright © 2015-2026 TargetMol Chemicals Inc. All Rights Reserved.