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Thermo Fisher Scientific NF-YA Polyclonal Antibody
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Thermo Fisher Scientific NF-YA Polyclonal Antibody

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NF-YA 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, WB, IHC, IP 등 다양한 응용에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 인간에 반응하고 마우스·랫·소에서도 반응 가능성이 있습니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 03. 오전 06:39
Thermo Fisher Scientific A302104A NF-YA Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
658,900원VAT 포함 724,790원
Thermo Fisher Scientific A302104AT NF-YA Polyclonal Antibody 10 ul pk판매 단위 pk ·
재고 확인 필요
194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific NF-YA Polyclonal Antibody

Thermo Fisher Scientific NF-YA Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) Assay-dependent
Immunohistochemistry (IHC) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:500–1:2,000
Immunoprecipitation (IP) 2–5 µg/mg lysate

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 320 and 333 of human nuclear transcription factor Y, alpha
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer Tris citrate/phosphate, pH 7–8
Contains 0.09% sodium azide
Storage Conditions 4°C
Shipping Conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • For IHC, epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections
  • Based on 100% sequence identity, this antibody is predicted to react with Mouse, Rat, and Bovine

Target Information

The SMN1 gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements, making it prone to rearrangements and deletions. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein, the survival motor neuron protein. The SMN complex plays a catalytic role in the assembly of small nuclear ribonucleoproteins, which are the building blocks of the spliceosome. Mutations in the SMN1 gene are known to cause spinal muscular atrophy types 1 and 2.


For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.

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