Thermo Fisher Scientific C9orf50 Polyclonal Antibody
Human C9orf50 단백질을 인식하는 Rabbit Polyclonal Antibody로, IHC(P)에서 1:200~1:500 희석으로 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol 버퍼에 보관. 연구용으로만 사용.
- 판매단위
- pk
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Applications
- Immunohistochemistry (Paraffin) (IHC (P)): 1:200–1:500
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant protein corresponding to Human C9orf50. Recombinant protein control fragment (Product #RP-93069) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.05 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_2639186 |
Product Specific Information
Immunogen sequence:
HSQFTTVRKA NQPHGAQVPR LKAALTHNPS GEGSRPCRQR CPFRVRFADE TLQDTTLRYW ERRRSVQQSV IVNQKAALPV ASERVFGSVG K
Highest antigen sequence identity to the following orthologs:
- Mouse: 47%
- Rat: 49%
Target Information
Chromosome 9 consists of about 145 million bases, representing 4% of the human genome and encoding nearly 900 genes. It plays a role in gender determination, with deletion of the distal portion of 9p potentially leading to male-to-female sex reversal.
Hereditary hemorrhagic telangiectasia, characterized by vascular defects, is associated with the chromosome 9 gene encoding endoglin protein (ENG). Familial dysautonomia is linked to chromosome 9 through the gene IKBKAP.
Chromosome 9 also contains the largest interferon family gene cluster and is involved in the translocation with chromosome 22 that produces the BCR-ABL fusion protein commonly found in leukemias.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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