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(R,Z)-12-(tert-butyldiphenylsilyloxy)octadec-9-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1346933-38-7

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1346933-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346933-38-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,9,3 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1346933-38:
(9*1)+(8*3)+(7*4)+(6*6)+(5*9)+(4*3)+(3*3)+(2*3)+(1*8)=177
177 % 10 = 7
So 1346933-38-7 is a valid CAS Registry Number.

1346933-38-7Relevant academic research and scientific papers

COMPOSITIONS AND METHODS FOR SILENCING APOLIPOPROTEIN B

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Paragraph 0644; 0649; 0650, (2013/05/22)

The present invention provides compositions and methods for the delivery of interfering RNAs such as siRNAs that silence APOB expression in cells such as liver cells. In particular, the nucleic acid-lipid particles provide efficient encapsulation of nucleic acids and efficient delivery of the encapsulated nucleic acid to cells such as liver cells in vivo. The compositions of the present invention are highly potent, thereby allowing effective knock-down of APOB at relatively low doses. In addition, the compositions and methods of the present invention are less toxic and provide a greater therapeutic index compared to compositions and methods previously known in the art.

NOVEL CATIONIC LIPIDS AND METHODS OF USE THEREOF

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Page/Page column 105, (2011/12/02)

The present invention provides compositions and methods for the delivery of therapeutic agents to cells. In particular, these include novel cationic lipids and nucleic acid-lipid particles that provide efficient encapsulation of nucleic acids and efficient delivery of the encapsulated nucleic acid to cells in vivo. The compositions of the present invention are highly potent, thereby allowing effective knock-down of a specific target protein at relatively low doses. In addition, the compositions and methods of the present invention are less toxic and provide a greater therapeutic index compared to compositions and methods previously known in the art.

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