- Search results for P98156
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6 products were found matching "P98156"!
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Item number: GSC-Z06401-100
VLDLR cerebellar hypoplasia (VLDLR-CH) is characterized by non-progressive congenital ataxia that is predominantly truncal and results in delayed ambulation, moderate-to-profound intellectual disability, dysarthria, strabismus, and seizures.VLDLR-CH is inherited in an autosomal recessive manner. Carrier testing for...
| Keywords: | Vldlr, Very low-density lipoprotein receptor |
| Origin: | mouse |
| MW: | 86.1 kD |
From 323.00€
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Item number: G-MOFI00316.96
| Application: | ELISA |
| Species reactivity: | mouse |
698.00€
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Item number: TGM-TMPK-00928-100ug
Description: VLDLR cerebellar hypoplasia (VLDLR-CH) is characterized by non-progressive congenital ataxia that is predominantly truncal and results in delayed ambulation, moderate-to-profound intellectual disability, dysarthria, strabismus, and seizures.VLDLR-CH is inherited in an autosomal recessive manner. Carrier...
| Keywords: | RP11-320E16.1, CHRMQ1, VLDLRCH, VLDLR, FLJ35024, VLDL-R |
| MW: | 86.1 kD |
From 284.00€
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NEW
Item number: TGM-TMPK-00928-10ug
Description: VLDLR cerebellar hypoplasia (VLDLR-CH) is characterized by non-progressive congenital ataxia that is predominantly truncal and results in delayed ambulation, moderate-to-profound intellectual disability, dysarthria, strabismus, and seizures.VLDLR-CH is inherited in an autosomal recessive manner. Carrier...
| Keywords: | VLDLR , FLJ35024 , VLDLRCH , RP11-320E16.1 , VLDL-R , CHRMQ1 |
| MW: | 86.1 kD |
From 38.00€
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Item number: L2601-35.50
VLDL R is a 105 kD type I integral membrane protein that belongs to the LDL receptor family. It plays a significant role in lipid metabolism and in nervous system development and function. 1,2 Mouse VLDL R has a 770 amino acid (aa) extracellular domain (ECD) and a 54 aa cytoplasmic region. The ECD contains eight...
| Keywords: | Vldlr, VLDL-R, VLDL receptor, Very low-density lipoprotein receptor |
| Origin: | mouse |
1,009.00€
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Item number: KT-VDR-MM101-100UG
Recombinant Mouse VLDLR Protein is expressed from HEK293 with His tag at the C-Terminus.It contains Gly28-Ser797. VLDLR cerebellar hypoplasia (VLDLR-CH) is characterized by non-progressive congenital ataxia that is predominantly truncal and results in delayed ambulation, moderate-to-profound intellectual disability,...
| Keywords: | VLDL-R, VLDLR, RP11-320E16.1, CHRMQ1, FLJ35024, VLDLRCH |
| Expressed in: | Human cells |
| Origin: | mouse |
| MW: | 86.1 kD |
From 219.00€
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