CacheBy
Thermo Fisher Scientific SMYD5 Polyclonal Antibody
원본

Thermo Fisher Scientific SMYD5 Polyclonal Antibody

상품 한눈에 보기

Human SMYD5 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, WB 및 IHC(P) 실험에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, 액상 형태로 제공되어 높은 특이성과 안정성을 보장합니다.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 05. 오전 05:45
Thermo Fisher Scientific PA561859 SMYD5 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific SMYD5 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.04–0.4 µg/mL
  • Publications: -

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:500–1:1,000
  • Publications: -

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human SMYD5. Recombinant protein control fragment (Product #RP-103042).
Conjugate Unconjugated
Form Liquid
Concentration 0.05 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, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2647668

Product Specific Information

Immunogen sequence:
MYCSAECRLA ATEQYHQVLC PGPSQDDPLH PLNKLQEAWR SIHYPPETAS IMLMARMVAT VKQAKDKDRW IRLFSQFCNK TANEEEEIVH KLLGDKFKG

Highest antigen sequence identity to orthologs:

  • Mouse: 82%
  • Rat: 91%

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.


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.