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Catalog Number: (103278-310)
Supplier: Novus Biologicals
Description: The Cav2.2 Antibody from Novus Biologicals is a rabbit polyclonal antibody to Cav2.2. This antibody reacts with human. The Cav2.2 Antibody has been validated for the following applications: Immunohistochemistry, Immunohistochemistry-Paraffin.


Catalog Number: (10244-642)
Supplier: Bioss
Description: The protein encoded by this gene is the pore-forming subunit of an N-type voltage-dependent calcium channel, which controls neurotransmitter release from neurons. The encoded protein forms a complex with alpha-2, beta, and delta subunits to form the high-voltage activated channel. This channel is sensitive to omega-conotoxin-GVIA and omega-agatoxin-IIIA but insensitive to dihydropyridines. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011].


Catalog Number: (10274-708)
Supplier: Bioss
Description: DBX2 is a 339 amino acid member of the H2.0 homeobox family. DBX2, which is localized to the nucleus, contains one homeobox DNA-binding domain, a region of 60 amino acids that binds DNA through a helix-turn-helix type of structure. DBX2, which is expressed in the forebrain, midbrain, hindbrain and spinal cord, has been implicated in CNS development.Specifically, DBX2 has been shown to play a role in spinal cord dorsal/ventral patterning, as well as the regionalization of the CNS. DBX2 is also thought to play a role in the production of multiple spinal cord cell types.


Catalog Number: (10316-048)
Supplier: Bioss
Description: HAPLN4.


Catalog Number: (10484-018)
Supplier: Bioss
Description: BRP44 is a 127 amino acid protein belonging to the UPF0041 family. The gene that encodes BRP44 maps to human chromosome 1, which is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.


Catalog Number: (470135-908)
Supplier: Wards
Description: Life size adult female human torso torso featuring an open back for in depth anatomical studies.


Catalog Number: (10325-516)
Supplier: Bioss
Description: Involved in cannabinoid-induced CNS effects. Acts by inhibiting adenylate cyclase. Could be a receptor for anandamide. Inhibits L-type Ca(2+) channel current. Isoform 2 and isoform 3 have altered ligand binding.


Catalog Number: (10206-162)
Supplier: Boster Biological Technology
Description: Mouse IgG monoclonal antibody for MAP1, microtubule-associated protein 1A (MAP1A) detection. Tested with WB, IHC-P, IHC-F in Rat. No cross reactivity with other proteins.


Catalog Number: (75931-580)
Supplier: Rockland Immunochemical
Description: RHEB control protein-HIS Epitope


Catalog Number: (10356-612)
Supplier: Bioss
Description: FAM3A (Family with sequence similarity 3, member A; MGC143089), [SUBCELLULAR LOCATION] Secreted. [TISSUE SPECIFICITY] In similar amounts in testis, pancreas, adrenal, placenta, brain, fetal brain, liver, kidney, skeletal muscle and heart. Belongs to the FAM3 family.


Catalog Number: (76073-436)
Supplier: Prosci
Description: For WB starting dilution is: 1:1000


Catalog Number: (89289-872)
Supplier: Genetex
Description: Rabbit polyclonal antibody to BRP44L


Catalog Number: (10356-614)
Supplier: Bioss
Description: FAM3A (Family with sequence similarity 3, member A; MGC143089), [SUBCELLULAR LOCATION] Secreted. [TISSUE SPECIFICITY] In similar amounts in testis, pancreas, adrenal, placenta, brain, fetal brain, liver, kidney, skeletal muscle and heart. Belongs to the FAM3 family.


Catalog Number: (10356-608)
Supplier: Bioss
Description: FAM3A (Family with sequence similarity 3, member A; MGC143089), [SUBCELLULAR LOCATION] Secreted. [TISSUE SPECIFICITY] In similar amounts in testis, pancreas, adrenal, placenta, brain, fetal brain, liver, kidney, skeletal muscle and heart. Belongs to the FAM3 family.


Supplier: Bachem Americas
Description: Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

Catalog Number: (10478-568)
Supplier: Bioss
Description: Probable transcription factor which exert its primary action widely during early neural development and in a very limited set of neurons in the mature brain.Defects in POU3F4 are a cause of deafness X-linked type 2 (DFNX2) . A mixed type of deafness characterized by both conductive hearing loss resulting from stapes (perilymphatic gusher) fixation and progressive sensorineural deafness.


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