Thermo Fisher Scientific CSH1 Recombinant Rabbit Monoclonal Antibody (7U9T2)
인간 CSH1 단백질을 인식하는 재조합 토끼 단클론 항체로, IHC, ICC/IF, ELISA에 적합합니다. HEK293 세포에서 발현되었으며, 고순도의 친화 크로마토그래피 정제 제품입니다. PBS/glycerol 완충액에 보관되며 -20°C에서 안정적으로 저장 가능합니다.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Immunohistochemistry (Paraffin) (IHC (P)) | 1:50–1:200 |
| Immunocytochemistry (ICC/IF) | 1:50–1:200 |
| ELISA | 1 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Expression System | HEK293 cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Clone | 7U9T2 |
| Immunogen | Synthetic peptide corresponding to amino acids 1–100 of human Placental lactogen (CSH1) (UniProt ID: P0DML2) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Affinity Chromatography |
| Storage Buffer | PBS, pH 7.3, with 50% glycerol, 0.05% BSA |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2911836 |
Product Specific Information
Immunogen sequence:
MAPGSRTSLL LAFALLCLPW LQEAGAVQTV PLSRLFDHAM LQAHRAHQLA IDTYQEFEET YIPKDQKYSF LHDSQTSFCF SDSIPTPSNM EETQQKSNLE
Target Information
The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones and plays an important role in growth control. The gene is located at the growth hormone locus on chromosome 17 along with four other related genes in the same transcriptional orientation, thought to have evolved by gene duplication. Although the five genes share high sequence identity, they are expressed selectively in different tissues. Alternative splicing generates additional isoforms, leading to further diversity. This family member is mainly expressed in the placenta and utilizes multiple transcription initiation sites. Expression of the identical mature proteins for chorionic somatomammotropin hormones 1 and 2 is upregulated during development, with the ratio of 1 to 2 increasing by term. Mutations in this gene result in placental lactogen deficiency and Silver-Russell syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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