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- Product number
- ABIN6218938 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-PSAP antibody
- Antibody type
- Polyclonal
- Description
- Affinity purification
- Reactivity
- Human, Mouse, Rat
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 20 μL
- Storage
- -20°C/-80°C
- Handling
- Avoid freeze / thaw cycles
Submitted references A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans.
Saposin proteins: structure, function, and role in human lysosomal storage disorders.
Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease.
Spiegel R, Bach G, Sury V, Mengistu G, Meidan B, Shalev S, Shneor Y, Mandel H, Zeigler M
Molecular genetics and metabolism 2005 Feb;84(2):160-6
Molecular genetics and metabolism 2005 Feb;84(2):160-6
Saposin proteins: structure, function, and role in human lysosomal storage disorders.
O'Brien JS, Kishimoto Y
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 1991 Mar 1;5(3):301-8
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 1991 Mar 1;5(3):301-8
Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease.
Schnabel D, Schröder M, Sandhoff K
FEBS letters 1991 Jun 17;284(1):57-9
FEBS letters 1991 Jun 17;284(1):57-9
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Supportive validation
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