Thermo Fisher Scientific SMYD5 Polyclonal Antibody
Thermo Fisher Scientific의 SMYD5 Polyclonal Antibody는 인간 SMYD5 단백질을 인식하는 토끼 유래 IgG 항체입니다. IHC(P) 및 ICC/IF 실험에 적합하며, 항원 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용 가능합니다.
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Applications
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:50–1:200
Immunocytochemistry (ICC/IF)
- Tested Dilution: 0.25–2 µg/mL
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-91632) |
| 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, store at -20°C avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2647667 |
Product Specific Information
Immunogen sequence:
QLELLRRLFT EALYEEAVSQ WFTPDGFRSL FALVGTNGQG IGTSSLSQWV HACDTLELKP QDREQLDAFI DQLYKDIEAA TGEFLNCEGS GLFVLQSCC
Highest antigen sequence identity to orthologs:
- Mouse: 91%
- Rat: 95%
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 linked to defects in ABCG5 and ABCG8 genes. Additionally, Alström syndrome, an extremely rare recessive genetic disorder, is caused by mutations in the ALMS1 gene on chromosome 2.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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