中文 
别名:Williams-Beuren syndrome chromosomal region 27 protein, WBSCR27应用:WB,IHC
反应种属:Human
规格：50μl/100μl
| Description |
|---|
| WBSCR27 encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. |
| Specification | |
|---|---|
| Aliases | Williams-Beuren syndrome chromosomal region 27 protein, WBSCR27 |
| Entrez GeneID | 155368 |
| Swissprot | Q8N6F8 |
| WB Predicted band size | 26.5kDa |
| Host/Isotype | Rabbit IgG |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human |
| Immunogen | This WBSCR27 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 5-34 amino acids from the N-terminal region of human WBSCR27. |
| Formulation | Purified polyclonal antibody supplied in PBS with 0.05% sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
| Application | |
|---|---|
| WB | 1/1000 |
| IHC | 1/100-1/500 |
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WBSCR27 Antibody (N-term) (Cat. #P30806) western blot analysis in NCI-H460 cell line lysates (35ug/lane).This demonstrates the WBSCR27 antibody detected the WBSCR27 protein (arrow). |
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WBSCR27 antibody (N-term) (Cat. #AP10548a) immunohistochemistry analysis in formalin fixed and paraffin embedded human hepatocarcinoma followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of the WBSCR27 antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated. |
本公司的所有产品仅用于科学研究或者工业应用等非医疗目的，不可用于人类或动物的临床诊断或治疗，非药用，非食用。
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本公司的所有产品仅用于科学研究或者工业应用等非医疗目的，不可用于人类或动物的临床诊断或治疗，非药用，非食用。
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