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Thermo Fisher Scientific SMYD5 Polyclonal Antibody
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Thermo Fisher Scientific SMYD5 Polyclonal Antibody

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SMYD5 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody입니다. Western blot 및 IHC(P)에서 사용 가능하며, 인간과 마우스에 반응합니다. 고순도 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공합니다. 연구용으로만 사용됩니다.

카탈로그번호
PA529153
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 05:09
Thermo Fisher Scientific PA529153 SMYD5 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
660,800원VAT 포함 726,880원

Thermo Fisher Scientific · Thermo Fisher Scientific SMYD5 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:3,000

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:100–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to a region within amino acids 305–401 of Human SMYD5
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7, with 1% BSA, 20% glycerol
Contains 0.01% thimerosal
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_2546629

Product Specific Information

  • Recommended positive controls: 293T, A431, H1299, HeLaS3, HepG2, Molt-4, Raji
  • Predicted reactivity: Mouse (100%), Rat (100%), Bovine (100%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

Retinoic acid (RA) represents the oxidized form of vitamin A and, via interactions with retinoic acid receptors (RARs), plays a crucial role in development, cellular growth and differentiation. The gene encoding RAI15 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin ichthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alström syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.


WARNING: This product can expose you to chemicals including mercury, which is known to the State of California to cause birth defects or other reproductive harm.
For more information, visit www.P65Warnings.ca.gov.

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


제품 이미지

(PA5-29153_SMYD5_Q6GMV2-1_Rabbit.svg 및 PA5-29153_SMYD5_Q6GMV2-1_Rabbit_PDP.jpeg 이미지 포함)

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