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Anti-TDRKH Antibody (6R551)
Catalog No. TMAB-13443 Copy Product Info
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Anti-TDRKH Antibody (6R551) is a Mouse antibody targeting TDRKH. Anti-TDRKH Antibody (6R551) can be used in WB.
Anti-TDRKH Antibody (6R551)
Copy Product Info🥰Excellent
Catalog No. TMAB-13443
Anti-TDRKH Antibody (6R551) is a Mouse antibody targeting TDRKH. Anti-TDRKH Antibody (6R551) can be used in WB.
Anti-TDRKH Antibody
(6R551)
(6R551)
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 25 μL | $151 | 7-10 days | 7-10 days | |
| 50 μL | $261 | 7-10 days | 7-10 days | |
| 100 μL | $473 | 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-TDRKH Antibody (6R551) is a Mouse antibody targeting TDRKH. Anti-TDRKH Antibody (6R551) can be used in WB. |
| Ig Type | IgG1, Kappa |
| Clone | 6R551 |
| Reactivity | Human (predicted:Mouse,Rat) |
| Verified Activity | Blocking buffer: 5% NFDM/TBST Primary ab dilution: 1:1000 Primary ab incubation condition: 2 hours at room temperature Secondary ab: Goat Anti-Mouse IgG H&L (HRP) Lysate: SH-SY5Y, Rat brain, Mouse brain, HeLa Protein loading quantity: 20 μg Exposure time: 3 s Predicted MW: 67-70 kDa Observed MW: 67-70 kDa |
| Application | |
| Recommended Dose | WB: 1:500-1000 |
| Antibody Type | Monoclonal |
| Host Species | Mouse |
| Subcellular Localization | Nucleus. |
| Tissue Specificity | Expressed in all tissues and cell lines examined. |
| Construction | Recombinant Antibody |
| Purification | Protein G purified |
| Appearance | Liquid |
| Formulation | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| Concentration | 1mg/ml |
| Research Background | Binding of FREAC-3 and FREAC-4 to their cognate sites results in bending of the DNA at an angle of 80-90 degrees. Involvement in disease; Defects in FOXC1 are the cause of Axenfeld-Rieger syndrome type 3 (RIEG3); also known as Axenfeld-Rieger syndrome (ARS) or Axenfeld syndrome or Axenfeld anomaly. It is characterized by posterior corneal embryotoxon, prominent Schwalbe line and iris adhesion to the Schwalbe line. Other features may be hypertelorism (wide spacing of the eyes), hypoplasia of the malar bones, congenital absence of some teeth and mental retardation. When associated with tooth anomalies, the disorder is known as Rieger syndrome. Glaucoma is a progressive blinding condition that occurs in approximately half of patients with Axenfeld-Rieger malformations. |
| Gene Name | FOXC1 |
| Gene ID | |
| Protein Name | Forkhead box protein C1 |
| Function | Binding of FREAC-3 and FREAC-4 to their cognate sites results in bending of the DNA at an angle of 80-90 degrees. |
| 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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