Secreted Frizzled-Related Protein 3 (FRZB) Antibody

195€ (20 µl)
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935106861
info@markelab.com
name
Secreted Frizzled-Related Protein 3 (FRZB) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx005056
tested applications
ELISA, WB
Description
FRZB Antibody is a Rabbit Polyclonal antibody against FRZB. The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Secreted Frizzled-Related Protein 3 (FRZB) |
| Host | Rabbit |
| Reactivity | Rat, Mouse |
| Recommended Dilution | ELISA: 1 µg/ml, WB: 1/2000 - 1/7000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified by affinity chromatography. |
| Size 1 | 20 µl |
| Size 2 | 100 µl |
| Size 3 | 2 × 100 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB |
| Buffer | PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q92765 |
| Gene ID | 2487 |
| NCBI Accession | NP_001454.2 |
| Background | Antibody anti-FRZB |
| Status | RUO |
| Note | Concentration: > 0.2 mg/ml - |
Descripción
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Soluble frizzled-related proteins(sFRPS) function as modulators of Wnt signaling through direct interaction with Wnts. They have a role in regulating cell growth and differentiation in specific cell types. SFRP3/FRZB appears to be involved in limb skeletogenesis. Antagonist of Wnt8 signaling. Regulates chondrocyte maturation and long bone development.
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Secreted Frizzled-Related Protein 3 (FRZB) Antibody
FRZB Antibody is a Rabbit Polyclonal antibody against FRZB. The protein encoded by this gene is a secreted protein that is involved in the regulation of bone development. Defects in this gene are a cause of female-specific osteoarthritis (OA) susceptibility.
Ver Producto