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Catalog Number: (10356-616)
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: (10356-618)
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: (470119-052)
Supplier: American 3B Scientific
Description: This six-part head is mounted on a base and features a removable four-part brain half with arteries.


Catalog Number: (76107-924)
Supplier: Bioss
Description: This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.


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.


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: (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: (89302-712)
Supplier: Genetex
Description: Rabbit polyclonal to BAALC (N-term)


Catalog Number: (10356-610)
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: (76107-926)
Supplier: Bioss
Description: This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.


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.


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: (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: (10326-316)
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: (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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