"Prosci"
Anti-GUCA2A Rabbit Polyclonal Antibody
Supplier: Prosci
Anti-GUCA2A Rabbit Polyclonal Antibody
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Anti-FABP3 Rabbit Monoclonal Antibody [clone: A10 ]
Supplier: Prosci
Anti-FABP3 Rabbit Monoclonal Antibody [clone: A10 ]
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Human KLRA1 Peptide (13 aa near C-terminus)
Supplier: Prosci
KLRA1 peptide is used for blocking the activity of KLRA1 antibody.
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Anti-BOS161721 Recombinant Antibody
Supplier: Prosci
Anti-BOS161721 Recombinant Antibody
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Anti-HK2 Rabbit Polyclonal Antibody
Supplier: Prosci
Hexokinases phosphorylate glucose to produce glucose-6-phosphate, thus committing glucose to the glycolytic pathway. HK2 (hexokinase 2) is the predominant form found in skeletal muscle. It localizes to the outer membrane of mitochondria. Expression of this protein is insulin-responsive, and studies in rat suggest that it is involved in the increased rate of glycolysis seen in rapidly growing cancer cells. Hexokinases phosphorylate glucose to produce glucose-6-phosphate, thus committing glucose to the glycolytic pathway. This gene encodes hexokinase 2, the predominant form found in skeletal muscle. It localizes to the outer membrane of mitochondria. Expression of this gene is insulin-responsive, and studies in rat suggest that it is involved in the increased rate of glycolysis seen in rapidly growing cancer cells. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
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Anti-PLA2R1 Rabbit Polyclonal Antibody
Supplier: Prosci
Anti-PLA2R1 Rabbit Polyclonal Antibody
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Thymus Lysate, ProSci
Supplier: Prosci
Thymus tissue lysate (Human) was prepared by homogenization in lysis buffer (10 mM HEPES pH7.9, 1.5 mM MgCl2, 10 mM KCl, 1 mM ethylenediaminetetraacetic acid, 10% glycerol, 1% NP-40, and a cocktail of protease inhibitors)
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Anti-CCBL2 Rabbit Polyclonal Antibody
Supplier: Prosci
RP11-82K18.3 is an aminotransferase that transaminates kynurenine to form kynurenic acid. Kynurenic acid is a metabolite of tryptophan.
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Anti-GRINA Rabbit Polyclonal Antibody
Supplier: Prosci
GRINA Antibody: The transmembrane BAX inhibitor motif (TMBIM) family of proteins includes the founder member TMBIM6/BI-1, TMBIM1/RECS1 (responsive to centrifugal force and shear stress gene 1 protein), TMBIM2/LFG (life guard), TMBIM3/GRINA (glutamate receptor ionotropic NMDA protein 1), TMBIM4/GAAP (Golgi anti-apoptotic-associated protein), and TMBIM5/GHTIM (growth hormone-inducible transmembrane protein). They are highly conserved in mammals and zebrafish and contain a conserved BAX inhibitor-1 motif. GRINA is expressed in the brain and is a potential apoptotic regulator.
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Anti-Klra6 Mouse Monoclonal Antibody [clone: [HBF-719]] (FITC (Fluorescein Isothiocyanate))
Supplier: Prosci
Anti-Klra6 Mouse Monoclonal Antibody [clone: [HBF-719]] (FITC (Fluorescein Isothiocyanate))
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Anti-NEK9 Rabbit Polyclonal Antibody
Supplier: Prosci
Anti-NEK9 Rabbit Polyclonal Antibody
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Anti-Mouse Monoclonal Antibody [clone: [21-1A4]] (PE (Phycoerythrin))
Supplier: Prosci
Anti-Mouse Monoclonal Antibody [clone: [21-1A4]] (PE (Phycoerythrin))
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Anti-JPH3 Rabbit Polyclonal Antibody
Supplier: Prosci
JPH3 Antibody: Junctional complexes between the plasma membrane (PM) and endoplasmic/sarcoplasmic reticulum (ER/SR) are a common feature of all excitable cell types and mediate cross talk between cell surface and intracellular ion channels. Junctophilins (JPs) are important components of the junctional complexes. JPs are composed of a carboxy-terminal hydrophobic segment spanning the ER/SR membrane and a remaining cytoplasmic domain that shows specific affinity for the PM. Four JPs have been identified as tissue-specific subtypes derived from different genes: JPH1 is expressed in skeletal muscle, JPH2 is detected throughout all muscle cell types, and JPH3 and JPH4 are predominantly expressed in the brain. In the CNS, both JPH3 and JPH4 are expressed throughout neural sites and contribute to the subsurface cistern formation in neurons. Mice lacking both JPH3 and JPH4 subtypes exhibit serious symptoms such as impaired learning and memory and are accompanied by abnormal nervous functions. A repeat expansion in JPH3 is associated with Huntington disease-like 2. At least two isoforms of JPH3 are known to exist.



