HOME3抗体应用：WB 1:500-2000This gene encodes a member of the HOMER family of postsynaptic density scaffolding proteins that share a similar domain structure consisting of an N-terminal Enabled/vasodilator-stimulated phosphoprotein homology 1 domain which mediates protein-protein interactions, and a carboxy-terminal coiled-coil domain and two leucine zipper motifs that are involved in self-oligomerization. The encoded protein binds numerous other proteins including group I metabotropic glutamate receptors, inositol 1,4,5-trisphosphate receptors and amyloid precursor proteins and has been implicated in diverse biological functions such as neuronal signaling, T-cell activation and trafficking of amyloid beta peptides. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Mar 2009],

HOMEZ抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:May function as a transcriptional regulator.,similarity:Contains 2 homeobox DNA-binding domains.,subunit:Homodimer or heterodimer (Potential). Interacts with HOXC8.,tissue specificity:Ubiquitous. Strongly expressed in adult testis and kidney as well as fetal lung and kidney.,

HP1B3抗体应用：WB 1:500-2000

HPGDS抗体应用：WB 1:500-2000 ELISA 1:5000-20000hematopoietic prostaglandin D synthase(HPGDS) Homo sapiens Prostaglandin-D synthase is a sigma class glutathione-S-transferase family member. The enzyme catalyzes the conversion of PGH2 to PGD2 and plays a role in the production of prostanoids in the immune system and mast cells. The presence of this enzyme can be used to identify the differentiation stage of human megakaryocytes. [provided by RefSeq, Jul 2008],

HPLN1抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Stabilizes the aggregates of proteoglycan monomers with hyaluronic acid in the extracellular cartilage matrix.,similarity:Belongs to the HAPLN family.,similarity:Contains 1 Ig-like V-type (immunoglobulin-like) domain.,similarity:Contains 2 Link domains.,tissue specificity:Widely expressed. Weakly expressed in the brain.,

HPLN4抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Binds to hyaluronic acid and may be involved in formation of the extracellular matrix.,similarity:Belongs to the HAPLN family.,similarity:Contains 1 Ig-like C2-type (immunoglobulin-like) domain.,similarity:Contains 2 Link domains.,tissue specificity:Expressed predominantly in brain.,

HPS5抗体应用：WB 1:500-2000 ELISA 1:5000-20000HPS5, biogenesis of lysosomal organelles complex 2 subunit 2(HPS5) Homo sapiens This gene encodes a protein that may play a role in organelle biogenesis associated with melanosomes, platelet dense granules, and lysosomes. This protein interacts with Hermansky-Pudlak syndrome 6 protein and may interact with the cytoplasmic domain of integrin, alpha-3. Mutations in this gene are associated with Hermansky-Pudlak syndrome type 5. Multiple transcript variants encoding two distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008],

HRCT1抗体应用：WB 1:500-2000

HRG抗体应用：WB 1:500-2000 ELISA 1:5000-20000histidine rich glycoprotein(HRG) Homo sapiens This histidine-rich glycoprotein contains two cystatin-like domains and is located in plasma and platelets. The physiological function has not been determined but it is known that the protein binds heme, dyes and divalent metal ions. The encoded protein also has a peptide that displays antimicrobial activity against C. albicans, E. coli, S. aureus, P. aeruginosa, and E. faecalis. It can inhibit rosette formation and interacts with heparin, thrombospondin and plasminogen. Two of the protein's effects, the inhibition of fibrinolysis and the reduction of inhibition of coagulation, indicate a potential prothrombotic effect. Mutations in this gene lead to thrombophilia due to abnormal histidine-rich glycoprotein levels. [provided by RefSeq, Nov 2014],

HRK抗体应用：WB 1:500-2000 ELISA 1:5000-20000harakiri, BCL2 interacting protein(HRK) Homo sapiens This gene encodes a member of the BCL-2 protein family. Members of this family are involved in activating or inhibiting apoptosis. The encoded protein localizes to intracellular membranes. This protein promotes apoptosis by interacting with the apoptotic inhibitors BCL-2 and BCL-X(L) via its BH3 domain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012],