
Thermo Fisher Scientific GALE Polyclonal Antibody
Thermo Fisher Scientific의 GALE Polyclonal Antibody는 인간, 생쥐, 랫트 반응성을 가지며 E. coli 유래 GALE 단백질을 면역원으로 제작된 토끼 IgG 항체입니다. Western blot 및 IHC에 적합하며, 항원 친화 크로마토그래피로 정제된 동결건조 형태로 제공됩니다. 연구용 전용 제품입니다.
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Applications
Western Blot (WB)
- Tested Dilution: 0.1–0.5 µg/mL
- Publications: References
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 0.5–1 µg/mL
- Publications: References
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host/Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | E. coli-derived human GALE recombinant protein (Position: M1–N340) |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 500 µg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS with 4 mg trehalose |
| Contains | 0.05 mg sodium azide |
| Storage Conditions | −20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2746412 |
Product Specific Information
Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 µg/mL.
Target Information
This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions:
- Epimerization of UDP-glucose to UDP-galactose
- Epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine
The bifunctional nature of the enzyme leads to metabolic consequences where mutant cells depend on exogenous galactose and N-acetylgalactosamine for glycoprotein and glycolipid synthesis.
Mutations in this gene cause epimerase-deficiency galactosemia (galactosemia type 3), characterized by liver damage, early-onset cataracts, deafness, and mental retardation, with severity ranging from mild (peripheral form) to severe (generalized form).
Multiple alternatively spliced transcripts encoding the same protein have been identified.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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