Thermo Fisher Scientific FAM221A Polyclonal Antibody
FAM221A 단백질을 인식하는 Rabbit Polyclonal 항체로 Western blot 및 IHC(Paraffin)에서 검증됨. 항원 친화 크로마토그래피로 정제되었으며 PBS/glycerol buffer에 보관. 인체 시료에 반응하며 연구용으로 적합.
- 카탈로그번호
- PA555403
- 판매단위
- pk
카탈로그
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 0.04–0.4 µg/mL |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:20–1:50 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human FAM221A. Recombinant protein control fragment (Product #RP-92837). |
| 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_2641388 |
Product Specific Information
Immunogen sequence:
DSPFLKAFQA SSSSSPETLT DVGTSSQVSS LRRPEEDDMA FFERRYQERM KMEKAAKWKG KAPLPSATK
Sequence identity (orthologs):
Mouse – 63%, Rat – 67%
Target Information
Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia, and Shwachman-Diamond syndrome.
Deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, characterized by mild mental retardation, friendliness with strangers, and an elfin appearance.
Deletions of portions of the q arm of chromosome 7 are also seen in several myeloid disorders, including acute myelogenous leukemia and myelodysplasia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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