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1621861-48-0

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1621861-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1621861-48-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,1,8,6 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1621861-48:
(9*1)+(8*6)+(7*2)+(6*1)+(5*8)+(4*6)+(3*1)+(2*4)+(1*8)=160
160 % 10 = 0
So 1621861-48-0 is a valid CAS Registry Number.

1621861-48-0Downstream Products

1621861-48-0Relevant articles and documents

Photoactivable Glycolipid Antigens Generate Stable Conjugates with CD1d for Invariant Natural Killer T Cell Activation

Veerapen, Natacha,Kharkwal, Shalu Sharma,Jervis, Peter,Bhowruth, Veemal,Besra, Amareeta K.,North, Simon J.,Haslam, Stuart M.,Dell, Anne,Hobrath, Judith,Quaid, Padraic J.,Moynihan, Patrick J.,Cox, Liam R.,Kharkwal, Himanshu,Zauderer, Maurice,Besra, Gurdyal S.,Porcelli, Steven A.

, p. 3161 - 3173 (2018/09/06)

Activation of invariant natural killer T lymphocytes (iNKT cells) by α-galactosylceramide (α-GC) elicits a range of pro-inflammatory or anti-inflammatory immune responses. We report the synthesis and characterization of a series of α-GC analogues with acyl chains of varying length and a terminal benzophenone. These bound efficiently to the glycolipid antigen presenting protein CD1d, and upon photoactivation formed stable CD1d-glycolipid covalent conjugates. Conjugates of benzophenone α-GCs with soluble or cell-bound CD1d proteins retained potent iNKT cell activating properties, with biologic effects that were modulated by acyl chain length and the resulting affinities of conjugates for iNKT cell antigen receptors. Analysis by mass spectrometry identified a unique covalent attachment site for the glycolipid ligands in the hydrophobic ligand binding pocket of CD1d. The creation of covalent conjugates of CD1d with α-GC provides a new tool for probing the biology of glycolipid antigen presentation, as well as opportunities for developing effective immunotherapeutics.

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