Maackiain
CAS No. 19908-48-6
Maackiain( —— )
Catalog No. M18198 CAS No. 19908-48-6
MAK1 is the second functional gene cloned from Maackiain detoxification.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 67 | In Stock |
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| 5MG | 60 | In Stock |
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| 10MG | 86 | In Stock |
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| 25MG | 140 | In Stock |
|
| 50MG | 200 | In Stock |
|
| 100MG | 296 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameMaackiain
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NoteResearch use only, not for human use.
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Brief DescriptionMAK1 is the second functional gene cloned from Maackiain detoxification.
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DescriptionMaackiain induces apoptosis and growth suppression MAK1 is the second functional gene cloned from Maackiain detoxification.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research AreaOthers-Field
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Indication——
Chemical Information
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CAS Number19908-48-6
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Formula Weight284.26
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Molecular FormulaC16H12O5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (879.48 mM)
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SMILESC1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Bursin
Bursin is a peptide that can be isolated from the bursa of Fabricius of chicken. Bursin induces the phenotypic differentiation of mammalian and avian B precursor cells. Bursin also increases cyclic guanosine monophosphate in cells of the human B-cell line Daudi, its derivatives are able to protect against infection by amplifying the immune response induced by H9N2.
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Dihydrorhodamine 123
Dihydrorhodamine 123 is a fluorescent probe.
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2-Methylsuccinic aci...
Methylsuccinic acid is a normal metabolite found in human fluids. Increased urinary levels of Methylsuccinic acid (together with ethylmalonic acid) are the main biochemical measurable features in ethylmalonic encephalopathy a rare metabolic disorder with an autosomal recessive mode of inheritance that is clinically characterized by neuromotor delay hyperlactic acidemia recurrent petechiae orthostatic acrocyanosis and chronic diarrhea.
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