
Thermo Fisher Scientific GALE Polyclonal Antibody
Rabbit polyclonal antibody against human GALE, validated for Western blot. Recognizes recombinant fragment (aa 107–326). High purity via antigen affinity chromatography. Suitable for multiple species and stored in glycerol buffer for stability.
- 카탈로그번호
- PA530037
- 판매단위
- pk
카탈로그
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Applications
- Western Blot (WB)
Tested Dilution
- 1:500–1:3,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant fragment corresponding to a region within amino acids 107–326 of Human GALE |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.58 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | 0.1M Tris glycine, pH 7, with 20% glycerol |
| Contains | 0.01% thimerosal |
| Storage Conditions | Store at 4°C short term; for long-term storage, store at -20°C, avoiding freeze/thaw cycles |
| Shipping Conditions | Wet ice |
| RRID | AB_2547511 |
Product Specific Information
- Recommended positive controls: A431, Raji
- Predicted reactivity: Mouse (93%), Rat (93%), Zebrafish (82%), Rhesus Monkey (98%), Bovine (97%)
- Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Target Information
UDP-galactose-4-epimerase catalyzes two analogous reactions: the epimerization of UDP-glucose to UDP-galactose and UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. This bifunctional enzyme is essential for glycoprotein and glycolipid synthesis. Mutations cause epimerase-deficiency galactosemia (galactosemia type 3), leading to liver damage, cataracts, deafness, and mental retardation. Multiple alternatively spliced transcripts encode the same protein.
⚠ WARNING: This product can expose you to chemicals including mercury, known to the State of California to cause birth defects or other reproductive harm. For more information, visit www.P65Warnings.ca.gov.
For Research Use Only. Not for use in diagnostic procedures or resale without express authorization.
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