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Anticorps
Numéro de catalogue:
(BOSSBS-13206R-A750)
Fournisseur:
Bioss
Description:
This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in myogenic growth and differentiation. Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13206R-FITC)
Fournisseur:
Bioss
Description:
This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in myogenic growth and differentiation. Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma. [provided by RefSeq].
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0408R-A488)
Fournisseur:
Bioss
Description:
Heamachrome
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0408R-A555)
Fournisseur:
Bioss
Description:
Heamachrome
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13206R-CY3)
Fournisseur:
Bioss
Description:
This gene belongs to the forkhead family of transcription factors which are characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it may play a role in myogenic growth and differentiation. Translocation of this gene with PAX3 has been associated with alveolar rhabdomyosarcoma. [provided by RefSeq].
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-19577R-A680)
Fournisseur:
Bioss
Description:
Chaperone protein which promotes assembly of the 20S proteasome as part of a heterodimer with PSMG2. The PSMG1-PSMG2 heterodimer binds to the PSMA5 and PSMA7 proteasome subunits, promotes assembly of the proteasome alpha subunits into the heteroheptameric alpha ring and prevents alpha ring dimerisation.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0243R-CY5)
Fournisseur:
Bioss
Description:
beta-expansin (EXBP2) may cause loosening and extension of plant cell walls by disrupting noncovalent bonding between cellulose microfibrils and matrix glucans. No enzymatic activity has been found Subcellular Location at Cell-wall bound. Belongs to the expansin family.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1957R-A555)
Fournisseur:
Bioss
Description:
Growth factor active in angiogenesis, vasculogenesis and endothelial cell growth. Induces endothelial cell proliferation, promotes cell migration, inhibits apoptosis and induces permeabilization of blood vessels. Binds to the FLT1/VEGFR1 and KDR/VEGFR2 receptors, heparan sulfate and heparin. NRP1/Neuropilin-1 binds isoforms VEGF-165 and VEGF-145. Isoform VEGF165B binds to KDR but does not activate downstream signaling pathways, does not activate angiogenesis and inhibits tumor growth.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0243R-A647)
Fournisseur:
Bioss
Description:
beta-expansin (EXBP2) may cause loosening and extension of plant cell walls by disrupting noncovalent bonding between cellulose microfibrils and matrix glucans. No enzymatic activity has been found Subcellular Location at Cell-wall bound. Belongs to the expansin family.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0243R-A488)
Fournisseur:
Bioss
Description:
beta-expansin (EXBP2) may cause loosening and extension of plant cell walls by disrupting noncovalent bonding between cellulose microfibrils and matrix glucans. No enzymatic activity has been found Subcellular Location at Cell-wall bound. Belongs to the expansin family.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0243R-CY5.5)
Fournisseur:
Bioss
Description:
beta-expansin (EXBP2) may cause loosening and extension of plant cell walls by disrupting noncovalent bonding between cellulose microfibrils and matrix glucans. No enzymatic activity has been found Subcellular Location at Cell-wall bound. Belongs to the expansin family.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1963R-CY3)
Fournisseur:
Bioss
Description:
Glandular kallikreins cleave Met-Lys and Arg-Ser bonds in kininogen to release Lys-bradykinin.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-1964R-CY5)
Fournisseur:
Bioss
Description:
Kallikreins are a subgroup of serine proteases having diverse physiological functions. Growing evidence suggests that many kallikreins are implicated in carcinogenesis and some have potential as novel cancer and other disease biomarkers. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Its protein product is a protease present in seminal plasma. It is thought to function normally in the liquefaction of seminal coagulum, presumably by hydrolysis of the high molecular mass seminal vesicle protein. Serum level of this protein, called PSA in the clinical setting, is useful in the diagnosis and monitoring of prostatic carcinoma. Alternate splicing of this gene generates several transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008].
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0498R-A488)
Fournisseur:
Bioss
Description:
Beta-adrenergic receptors mediate the catecholamine-induced activation of adenylate cyclase through the action of G proteins. This receptor binds epinephrine and norepinephrine with approximately equal affinity. Mediates Ras activation through G(s)-alpha- and cAMP-mediated signaling.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-0498R-FITC)
Fournisseur:
Bioss
Description:
Beta-adrenergic receptors mediate the catecholamine-induced activation of adenylate cyclase through the action of G proteins. This receptor binds epinephrine and norepinephrine with approximately equal affinity. Mediates Ras activation through G(s)-alpha- and cAMP-mediated signaling.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13265R-A750)
Fournisseur:
Bioss
Description:
GALE is a 348 amino acid protein that functions as the third enzyme in the Leloir pathway of galactose metabolism. A member of the sugar epimerase family, GALE exists as a homodimer, binds FAD as a cofactor and catalyzes the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine and UDP-glucose to UDP-galactose. The gene encoding GALE maps to human chromosome 1p36.11 and mutations in this gene lead to the development of complex disorder known as epimerase-deficiency galactosemia (EDG) or galactosemia type 3, which is characterized by mental retardation, liver damage, cataracts and deafness.
UOM:
1 * 100 µl
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