
Thermo Fisher Scientific BRPF1 Recombinant Superclonal Antibody (19HCLC)
BRPF1 단백질을 인식하는 Thermo Fisher의 Recombinant Superclonal™ 항체로, 인간에 반응하며 마우스, 랫, 보바인에도 예측 반응합니다. 폴리클로날의 민감도와 모노클로날의 특이성을 결합한 재조합 항체로 일관된 성능을 제공합니다. Western blot에 적합합니다.
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- Antibodies
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Applications
- Western Blot (WB): 1:250
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Expression System | Expi293 |
| Class | Recombinant Superclonal |
| Type | Antibody |
| Clone | 19HCLC |
| Immunogen | Protein corresponding to human BRPF1 (aa1–aa100) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Protein A |
| Storage Buffer | PBS, pH 7.4 |
| Contains | 0.09% sodium azide |
| Storage Conditions | Store at 4°C short term. For long term, store at -20°C. Avoid freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2811737 |
Product Specific Information
This antibody is predicted to react with Mouse, Rat, and Bovine.
Recombinant rabbit Superclonal™ antibodies are unique offerings from Thermo Fisher Scientific. They consist of a selection of multiple different recombinant monoclonal antibodies, combining the sensitivity of polyclonal antibodies with the specificity of monoclonal antibodies, while maintaining the consistency of recombinant production.
Functionally similar to polyclonal antibodies—recognizing multiple epitope sites and providing higher detection sensitivity for low-abundance targets—Superclonal™ antibodies have a defined mixture of light and heavy chains that can be reproduced in every lot, eliminating biological variability.
Note: Formerly called “Recombinant polyclonal antibody,” this product is now rebranded as “Recombinant Superclonal™ antibody.” The physical product and performance remain unchanged.
Target Information
BRPF1 (peregrin) is a component of the MOZ/MORF complex, which has histone H3 acetyltransferase activity. BRPF1 preferentially mediates histone H3-K23 acetylation and positively regulates transcription of RUNX1 and RUNX2. Mutations in this gene can result in intellectual developmental disorder with dysmorphic facies and ptosis.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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