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Thermo Fisher Scientific Hemoglobin alpha (2 chain) Recombinant Rabbit Monoclonal Antibody (HBA/9193R)
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Thermo Fisher Scientific Hemoglobin alpha (2 chain) Recombinant Rabbit Monoclonal Antibody (HBA/9193R)

상품 한눈에 보기

인간 HBA2 단백질을 인식하는 재조합 토끼 단클론 항체로, IHC(P) 실험에 적합합니다. 높은 특이성과 재현성을 제공하며, Protein A/G로 정제된 액상 형태입니다. PBS 및 BSA 완충액에 보존되어 연구용으로 사용됩니다.

카탈로그번호
3039-RBM4-Px (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 04. 오후 10:17
Thermo Fisher Scientific 3039-RBM4-P1 Hemoglobin alpha (2 chain) Recombinant Rabbit Monoclonal Antibody (HBA/9193R) 100 ug pk판매 단위 pk ·
재고 확인 필요
1,046,500원VAT 포함 1,151,150원
Thermo Fisher Scientific 3039-RBM4-P0 Hemoglobin alpha (2 chain) Recombinant Rabbit Monoclonal Antibody (HBA/9193R) 20 ug pk판매 단위 pk ·
재고 확인 필요
484,200원VAT 포함 532,620원

Thermo Fisher Scientific · Thermo Fisher Scientific Hemoglobin alpha (2 chain) Recombinant Rabbit Monoclonal Antibody (HBA/9193R)

Applications

  • Immunohistochemistry (Paraffin) (IHC (P)): 1–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG, kappa
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone HBA/9193R
Immunogen Recombinant fragment (around aa1–100) of human HBA2 protein
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Positive Control: Human spleen, lung, or placenta; stomach cancer
  • Cellular Location: Extracellular space

Target Information

HBA2 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 5untranslated regions and the introns, but they differ 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 constitute 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 as well as deletions of 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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