
Thermo Fisher Scientific Hemoglobin alpha Recombinant Rabbit Monoclonal Antibody (SN70-09)
Hemoglobin alpha 단백질을 검출하기 위한 recombinant rabbit monoclonal antibody (SN70-09). Western blot 및 IHC(P) 응용에 적합하며, 높은 특이성과 재현성을 제공. Protein A 정제 및 glycerol buffer로 안정적 보관 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 1:500–1:1,000
- View 1 publication
Immunohistochemistry (IHC)
- Tested Dilution: –
- View 1 publication
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:50–1:100
- View publication
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Published Species | Mouse |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | SN70-09 |
| Immunogen | Synthetic peptide within Human HBA1 aa 71–120 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage Buffer | TBS, pH 7.4, with 40% Glycerol, 0.05% BSA |
| Contains | 0.05% sodium azide |
| Storage Conditions | Store at 4°C short term; for long term, store at -20°C (avoid freeze/thaw cycles) |
| Shipping Conditions | Wet ice |
| RRID | AB_2809609 |
Product Specific Information
Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. Antibody DNA sequences from immunoreactive rabbits are cloned and screened to select optimal candidates.
Advantages include:
- Enhanced specificity and sensitivity
- Lot-to-lot consistency
- Animal origin-free formulation
- Broader immunoreactivity due to rabbit immune repertoire
Target Information
The human alpha globin gene cluster on chromosome 16 spans approximately 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 but differ in untranslated and intron regions.
Two alpha chains plus two beta chains form HbA, which constitutes ~97% of adult hemoglobin. Alpha chains combine with delta chains to form HbA2, and with gamma chains to form HbF.
Alpha thalassemias result from deletions of one or both alpha genes (HBA2 and HBA1) or from non-deletion mutations.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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