Thermo Fisher Scientific FAM13B Polyclonal Antibody
FAM13B 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. 인간 시료에 반응하며, IHC(P)에서 1:50–1:200 희석으로 사용 가능. 항원 친화 크로마토그래피로 정제된 액상형 항체로, 안정적인 장기 보관 가능.
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Applications
- Immunohistochemistry (Paraffin) (IHC (P)): 1:50–1:200
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant Human FAM13B. Recombinant protein control fragment (Product #RP-107851) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.2 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_2664980 |
Product Specific Information
Immunogen sequence:
YSLLKFLCRFL ANVASHHEEI WSANSLAAVF GPDVFHIYTD VEDMKEQEIV SRIMAGLLEN YYEFFENEEE DFSSNDLSSI
Highest antigen sequence identity to the following orthologs: mouse 100%, rat 100%.
Target Information
FAM13B is a 915 amino acid protein encoded by a gene located on human chromosome 5.
Chromosome 5 contains approximately 181 million base pairs and around 1,000 genes, representing about 6% of human genomic DNA.
It is associated with several genetic conditions, including:
- Cockayne syndrome (ERCC8 gene)
- Familial adenomatous polyposis (APC gene)
- Treacher Collins syndrome (TCOF1 gene)
- Cri du chat syndrome (deletion of p arm of chromosome 5)
- Therapy-related acute myelogenous leukemias and myelodysplastic syndrome (deletion of 5q or entire chromosome 5)
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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