Thermo Fisher Scientific CT47 Polyclonal Antibody
CT47 단백질을 검출하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot 및 IHC(P) 적용 가능. 인간 및 비인간 영장류 반응성. 고순도 친화 크로마토그래피 정제, 액상 형태로 -20°C 보관.
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Thermo Fisher Scientific CT47 Polyclonal Antibody
Applications and Tested Dilution
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:1,000–1:3,000 |
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Non-human primate |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | A synthesized peptide derived from human CT47A1–CT47A12 (Accession Q5JQC4), corresponding to amino acid residues T250–T288 |
| 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_2852677 |
Product Specific Information
Antibody detects endogenous levels of total CT47A.
Target Information
CT47 (Cancer/Testis Antigen Family 47) is a 288 amino acid protein strongly expressed in testis and weakly expressed in placenta and brain.
The CT47 gene is located on the human X chromosome, which contains about 153 million base pairs and nearly 1,000 genes.
Abnormal numbers or combinations of sex chromosomes can lead to conditions such as:
- Klinefelter’s syndrome (extra X chromosome with Y)
- Turner’s syndrome (single X chromosome)
- Triple X syndrome (more than two X chromosomes without Y)
Other X-linked conditions include color blindness, hemophilia, and Duchenne muscular dystrophy, which occur more frequently in males due to their single X chromosome.
Usage Notice
For Research Use Only. Not for use in diagnostic procedures.
Not for resale without express authorization.
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