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Thermo Fisher Scientific Hemoglobin Monoclonal Antibody (7A4)
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인간 헤모글로빈을 특이적으로 인식하는 Mouse IgG1 단일클론 항체입니다. ELISA, IP, RIA 등 다양한 면역분석에 사용 가능하며, 단백질 A로 정제된 액상 형태로 제공됩니다. 2–8°C 보관 시 6개월 안정하며 장기 보관은 -20°C 권장됩니다.
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- pk
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마지막 업데이트 2025. 08. 05. 오후 04:14
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Thermo Fisher Scientific MA514708 Hemoglobin Monoclonal Antibody (7A4) 100 ug pk판매 단위 pk ·
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713,600원VAT 포함 784,960원
Thermo Fisher Scientific · Thermo Fisher Scientific Hemoglobin Monoclonal Antibody (7A4)
Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| ELISA (ELISA) | Assay-dependent |
| Immunoprecipitation (IP) | Assay-dependent |
| Radioimmune Assays (RIA) | Assay-dependent |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | 7A4 |
| Immunogen | Human Hemoglobin |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage buffer | PBS, pH 7.4, with 1 mg/mL BSA |
| Contains | 0.05% sodium azide |
| Storage conditions | Maintain refrigerated at 2–8°C for up to 6 months. For long-term storage, store at -20°C. |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_10980945 |
Product Specific Information
- MA5-14708 targets Hemoglobin in ELISA, IP, and RIA applications and shows reactivity with Human samples.
- The immunogen is human Hemoglobin.
- Detects Hemoglobin with a predicted molecular weight of approximately 16 kDa.
- Product MA5-14708 is a smaller package size of MIH9505 (formerly sold as a Seradyn product).
Target Information
The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci:
5′- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3′.
- The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical.
- These genes differ slightly over the 5′ untranslated regions and introns, but significantly over the 3′ untranslated regions.
- Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of total hemoglobin.
- Alpha chains combine with delta chains to form HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin.
- Alpha thalassemias result from deletions of each of the alpha genes or both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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