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Thermo Fisher Scientific NFYA Polyclonal Antibody
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Thermo Fisher Scientific NFYA Polyclonal Antibody

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Thermo Fisher Scientific의 NFYA Polyclonal Antibody는 인간 NFYA 단백질을 인식하는 토끼 다클론 항체입니다. Western blot, IHC 및 ICC/IF 실험에 적합하며 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용됩니다.

카탈로그번호
PA584030
판매단위
pk
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마지막 업데이트 2025. 07. 31. 오전 10:46
Thermo Fisher Scientific PA584030 NFYA Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
740,000원VAT 포함 814,000원

Thermo Fisher Scientific · Thermo Fisher Scientific NFYA Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human NFYA. Recombinant protein control fragment (Product #RP-89282).
Conjugate Unconjugated
Form Liquid
Concentration 0.1 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_2791182

Product Specific Information

Immunogen sequence:
ANTNTTSSGQ GTVTVTLPVA GNVVNSGGMV MMVPGAGSVP AIQRIPLPGA EMLEEEPLYV NAKQYHRILK RRQARAKLEA EGKIPKERRK YLHESRHRHA MARKRGEGGR FFSPKEKDSP HMQDPNQADE E

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 catalyst 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 1/2.


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

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