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Thermo Fisher Scientific Hemoglobin alpha-1 Polyclonal Antibody
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Thermo Fisher Scientific Hemoglobin alpha-1 Polyclonal Antibody

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인간 Hemoglobin alpha-1을 인식하는 Rabbit Polyclonal Antibody로 Western blot 및 IHC(P) 검증 완료. 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공. 연구용으로만 사용 가능하며 장기 보관 시 -20°C 권장.

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마지막 업데이트 2025. 08. 05. 오전 03:27
Thermo Fisher Scientific PA560507 Hemoglobin alpha-1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific Hemoglobin alpha-1 Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human Hemoglobin. Recombinant protein control fragment (Product #RP-104362)
Conjugate Unconjugated
Form Liquid
Concentration 0.10 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% 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_2642387

Product Specific Information

Immunogen sequence:
MVLSPADKTN VKAAWGKVGA HAGEYGAEAL ERMFLSF

Highest antigen sequence identity to the following orthologs:

  • Mouse: 76%
  • Rat: 70%

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 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 the 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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