Thermo Fisher Scientific FAM221A Polyclonal Antibody
Human FAM221A 단백질에 특이적인 Rabbit Polyclonal Antibody로, WB, IHC(P), ICC/IF 등 다양한 응용에 적합. 항원 친화 크로마토그래피로 정제되었으며, 높은 특이성과 안정성 제공. 연구용으로만 사용 가능.
- 판매단위
- pk
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 0.04–0.4 µg/mL |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
| Immunocytochemistry (ICC/IF) | 0.25–2 µg/mL |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human FAM221A. Recombinant protein control fragment (Product #RP-92835). |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.9 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_2641389 |
Product Specific Information
Immunogen sequence:
MERLTLPLGG AAAVDEYLEY RRIVGEDDGG KLFTPEEYEE YKRKVLPLRL QNRLFVSWRS PTGMDCKLVG PET
Antigen sequence identity:
- Mouse: 95%
- Rat: 95%
Target Information
Chromosome 7 has been linked to multiple genetic conditions such as Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia, and Shwachman-Diamond syndrome.
Deletions of portions of the q arm of chromosome 7 are associated with Williams-Beuren syndrome and various 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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