
Thermo Fisher Scientific Aldolase A Recombinant Superclonal Antibody
Aldolase A 단백질을 인식하는 Thermo Fisher Scientific의 Recombinant Superclonal 항체로, 인간·마우스·랫트 반응성 확인됨. WB 및 ICC/IF에 사용 가능하며, 높은 특이성과 재현성을 제공. 단백질 A 정제, 액상 형태, 장기 보관 시 -20°C 권장.
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Applications
Western Blot (WB)
- Tested Dilution: 1–3 µg/mL
Immunocytochemistry (ICC/IF)
- Tested Dilution: 5 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Expression System | Expi293 |
| Class | Recombinant Superclonal |
| Type | Antibody |
| Immunogen | Peptides corresponding to human Aldolase (1) aa341–aa360, (2) aa84–aa103 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Protein A |
| Storage Buffer | PBS, pH 7.4 |
| Contains | 0.09% sodium azide |
| 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_2716906 |
Product Specific Information
This antibody is predicted to react with Monkey, Cat, Rabbit.
Recombinant rabbit Superclonal™ antibodies are unique offerings from Thermo Fisher Scientific. They are composed of multiple different recombinant monoclonal antibodies, combining the sensitivity of polyclonal antibodies with the specificity of monoclonal antibodies, and offering consistent performance across lots. These antibodies recognize multiple epitopes on the target, providing enhanced detection sensitivity for low-abundance targets.
Note: Formerly called “Recombinant polyclonal antibody”, now rebranded as “Recombinant Superclonal™ antibody”. The product and performance remain unchanged.
Target Information
Aldolase encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded enzyme catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate.
Three aldolase isozymes (A, B, and C) are encoded by distinct genes and are differentially expressed during development. Mutations in this gene are associated with Glycogen Storage Disease XII, an autosomal recessive disorder linked to hemolytic anemia. Disruption of this gene contributes to progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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