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Thermo Fisher Scientific Hemoglobin Monoclonal Antibody (7A4)
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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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마지막 업데이트 2025. 08. 05. 오후 04:14
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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