Antibody data
- Antibody Data
 - Antigen structure
 - References [3]
 - Comments [0]
 - Validations [0]
 
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Validation data
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- Product number
 - HPA023646 - Provider product page

 - Provider
 - Atlas Antibodies
 - Proper citation
 - Atlas Antibodies Cat#HPA023646, RRID:AB_1855741
 - Product name
 - Anti-PROSC
 - Antibody type
 - Polyclonal
 - Description
 - Polyclonal Antibody against Human PROSC, Gene description: proline synthetase co-transcribed homolog (bacterial), Validated applications: WB, IHC, Uniprot ID: O94903, Storage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.
 - Reactivity
 - Human
 - Host
 - Rabbit
 - Conjugate
 - Unconjugated
 - Isotype
 - IgG
 - Vial size
 - 100 µl
 - Concentration
 - 0.05 mg/ml
 - Storage
 - Store at +4°C for short term storage. Long time storage is recommended at -20°C.
 - Handling
 - The antibody solution should be gently mixed before use.
 
Submitted references		Maintenance of cellular vitamin B6 levels and mitochondrial oxidative function depend on pyridoxal 5′-phosphate homeostasis protein
				
A founder mutation in the PLPBP gene in families from Saguenay‐Lac‐St‐Jean region affected by a pyridoxine‐dependent epilepsy
				
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy
				
		
	
			Ciapaite J, van Roermund C, Bosma M, Gerrits J, Houten S, IJlst L, Waterham H, van Karnebeek C, Wanders R, Zwartkruis F, Jans J, Verhoeven-Duif N
Journal of Biological Chemistry 2023;299(9):105047
		Journal of Biological Chemistry 2023;299(9):105047
A founder mutation in the PLPBP gene in families from Saguenay‐Lac‐St‐Jean region affected by a pyridoxine‐dependent epilepsy
			Pal M, Lace B, Labrie Y, Laflamme N, Rioux N, Setty S, Dugas M, Gosselin L, Droit A, Chrestian N, Rivest S
JIMD Reports 2021;59(1):32-41
		JIMD Reports 2021;59(1):32-41
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy
			Darin N, Reid E, Prunetti L, Samuelsson L, Husain R, Wilson M, El Yacoubi B, Footitt E, Chong W, Wilson L, Prunty H, Pope S, Heales S, Lascelles K, Champion M, Wassmer E, Veggiotti P, de Crécy-Lagard V, Mills P, Clayton P
The American Journal of Human Genetics 2016;99(6):1325-1337
		The American Journal of Human Genetics 2016;99(6):1325-1337
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