GTX46325
IMPAD1 antibody, N-term
Cannot supply to this region.
- SKU:
- GTX46325
- Additional Names:
- inositol monophosphatase domain containing 1 , GPAPP , IMP 3 , IMP-3 , IMPA3
- Application:
- WB
- Concentration:
- 0.5-1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 2% Sucrose, 0.09% Sodium azide.
- Immunogen:
- A synthetic peptide corresponding to a N-terminal region of Human IMPAD1
- Uniprot:
- Q9NX62
- Synonyms:
- Golgi 3-prime phosphoadenosine 5-prime phosphate 3-prime phosphatase;Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase;golgi-resident nucleotide phosphatase;golgi-resident PAP phosphatase;GPAPP;IMP 3;IMP-3;IMPA3;IMPAD1;IMPase 3;inositol monophosphatase domain containing 1;inositol monophosphatase domain-containing protein 1;inositol-1(or 4)-monophosphatase 3;myo-inositol monophosphatase A3;phosphoadenosine phosphate 3'-nucleotidase
- Extra Details:
- 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. [provided by RefSeq, Dec 2011]
- Shipping Conditions:
- Blue Ice