Thermo Fisher Scientific ALDH3B2 Polyclonal Antibody
Thermo Fisher Scientific의 ALDH3B2 Polyclonal Antibody는 인간 ALDH3B2 단백질을 인식하는 토끼 유래 항체로, WB, IHC, ICC/IF에 사용 가능. 1 mg/mL 농도의 액상 형태로 PBS 버퍼에 보관되며, 알데하이드 대사 관련 연구용으로 적합.
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:1,000–1:3,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
| Immunocytochemistry (ICC/IF) | 1:100–1:500 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | A synthesized peptide derived from human ALDH3B2 (Accession P48448), corresponding to amino acid residues F338–L385 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage Buffer | PBS, pH 7.4, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C |
| Shipping Conditions | Wet ice |
| RRID | AB_2852925 |
Product Specific Information
Antibody detects endogenous levels of total ALDH3B2.
Target Information
ALDH3B2 (aldehyde dehydrogenase 3 family, member B2), also known as ALDH8, is a 385 amino acid protein that belongs to the ALDH family and is involved in alcohol metabolism. It is expressed in salivary gland tissue and catalyzes the NADP⁺-dependent conversion of an aldehyde into an acid. The gene encoding ALDH3B2 maps to human chromosome 11, which contains over 1,400 genes and comprises nearly 4% of the human genome. Several syndromes such as Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome are associated with defects in genes mapped to chromosome 11.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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(이미지 파일: PA5-103589_ALDH3B2_P48448-1_Rabbit.svg, PA5-103589_ALDH3B2_P48448-1_Rabbit_PDP.jpeg)
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