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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 토끼 폴리클로날 항체로, IHC 및 IHC-P에 적합합니다. Human과 Mouse에 반응하며, 항원 친화 크로마토그래피로 정제되었습니다. 4°C 보관, 연구용 전용입니다.

카탈로그번호
IHC00576x (2개 옵션)
판매단위
pk
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카탈로그

2개 옵션
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마지막 업데이트 2025. 08. 05. 오후 05:20
Thermo Fisher Scientific IHC00576 NF-YA Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
698,000원VAT 포함 767,800원
Thermo Fisher Scientific IHC00576T 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

Applications

Immunohistochemistry (IHC)

  • Tested Dilution: 1:100–1:500

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:100–1:500

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 333 and 347 of human nuclear transcription factor Y, alpha
Conjugate Unconjugated
Form Liquid
Concentration 0.25 mg/mL
Purification Antigen affinity chromatography
Storage Buffer TBS, pH 7.0–8.0, with 0.1% BSA
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
  • Based on 100% sequence identity, this antibody is predicted to react with Rat, Bovine, Dog, Horse, Rabbit, Guinea pig, Pig, Panda, Orangutan, Monkey, Gorilla, Chimpanzee, and Crab-eating macaque

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 which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein — survival motor neuron protein. The SMN complex plays a catalytic role in the assembly of small nuclear ribonucleoproteins, 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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