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Thermo Fisher Scientific Hemoglobin alpha Recombinant Rabbit Monoclonal Antibody (SN70-09)
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Thermo Fisher Scientific Hemoglobin alpha Recombinant Rabbit Monoclonal Antibody (SN70-09)

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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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마지막 업데이트 2025. 08. 01. 오후 08:31
Thermo Fisher Scientific MA532328 Hemoglobin alpha Recombinant Rabbit Monoclonal Antibody (SN70-09) 100 ul pk판매 단위 pk ·
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622,700원VAT 포함 684,970원

Thermo Fisher Scientific · Thermo Fisher Scientific Hemoglobin alpha Recombinant Rabbit Monoclonal Antibody (SN70-09)

Applications

Western Blot (WB)

Immunohistochemistry (IHC)

Immunohistochemistry (Paraffin) (IHC (P))


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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