IMPAD1 antibody (AA 81-180) (Biotin)
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- Target See all IMPAD1 Antibodies
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
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Binding Specificity
- AA 81-180
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This IMPAD1 antibody is conjugated to Biotin
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Predicted Reactivity
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human IMPAD1
- Isotype
- IgG
- Top Product
- Discover our top product IMPAD1 Primary Antibody
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- Application Notes
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C for 12 months.
- Expiry Date
- 12 months
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- Target
- IMPAD1 (Inositol Monophosphatase Domain Containing 1 (IMPAD1))
- Alternative Name
- IMPAD1 (IMPAD1 Products)
- Background
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Synonyms: IMP 3, IMPA3, IMPase 3, Inositol monophosphatase domain containing protein 1, Myo inositol monophosphatase A3.
Background: This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP). Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
- Gene ID
- 54928
- Pathways
- Glycosaminoglycan Metabolic Process
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