Product Name: HISPPD1 Antibody
Species Reactivity: Human, Mouse
Tested Applications: ELISA, WB
Applications: HISPPD1 antibody can be used for detection of HISPPD1 by ELISA at 1:1562500. HISPPD1 antibody can be used for detection of HISPPD1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 – 100,000.
User Note: Optimal dilutions for each application to be determined by the researcher.
Predicted Molecular Weight: 138 kDa
Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human HISPPD1.
Host Species: Rabbit
Purification: Antibody is purified by peptide affinity chromatography method.
Physical State: Lyophilized
CAS NO.: 349085-82-1
Product: MRE-269
Buffer: Antibody is lyophilized in PBS buffer with 2% sucrose. Add 50 μL of distilled water. Final antibody concentration is 1 mg/mL.
Concentration: 1 mg/ml
Storage Conditions: For short periods of storage (days) store at 4˚C. For longer periods of storage, store HISPPD1 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: HISPPD1, FLJ21506, KIAA0433, PPIP5K2, VIP2, IP7K2, HISPPD1
Accession NO.: NP_056031
Protein Ino: 41281583
Official Symbol: PPIP5K2
Geneid: 23262
Background: Inositol phosphates (IPs) and diphosphoinositol phosphates (PP-IPs), also known as inositol pyrophosphates, act as cell signaling molecules. HISPPD1 has both IP6 kinase (EC 2.7.4.21) and PP-IP5 (also called IP7) kinase (EC 2.7.4.24) activities that produce the high-energy pyrophosphates PP-IP5 and PP2-IP4 (also called IP8), respectively.Inositol phosphates (IPs) and diphosphoinositol phosphates (PP-IPs), also known as inositol pyrophosphates, act as cell signaling molecules. HISPPD1 has both IP6 kinase (EC 2.7.4.21) and PP-IP5 (also called IP7) kinase (EC 2.7.4.24) activities that produce the high-energy pyrophosphates PP-IP5 and PP2-IP4 (also called IP8), respectively (Fridy et al., 2007 [PubMed 17690096]).
PubMed ID:http://aac.asm.org/content/22/4/709.abstract
