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          • Primary Antibodies ›
          • RNF3 Antibodies

          Bioss

          PCGF3 Polyclonal Antibody

          View all (10) RNF3 antibodies

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          Cite PCGF3 Polyclonal Antibody

          Additional Information:
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          {{$ctrl.isSkuNotesCollapsed ? 'View more' : 'View less'}}

          Product Details

          BS-9169R

          Applications
          Tested Dilution
          Publications

          Western Blot (WB)

          1:500-1:2,000
          -

          Immunohistochemistry (Paraffin) (IHC (P))

          1:100-1:500
          -
          Product Specifications

          Species Reactivity

          Human, Mouse, Rat

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          KLH conjugated synthetic peptide derived from human PCGF3.

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          1 mg/mL

          Amount

          100 µg

          Purification

          Protein A

          Storage buffer

          0.01M TBS, pH 7.4, with 1% BSA, 50% glycerol

          Contains

          0.02% ProClin 300

          Storage conditions

          -20°C

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          Target Information

          Phosphorylase kinase is a hexadecameric enzyme that is comprised of four copies of four subunits that are encoded by four separate genes: PHKA, PHKB, PHKG, and PH kDa. This serine/threonine specific kinase converts glycogen phosphorylase b to glycogen phosphorylase a, resulting in the release of glucose-1-phophate from glycogen. PHKB (Phosphorylase b kinase regulatory subunit beta) is a 1093 amino acid subunit of phosphorylase kinase that, along with PHKA, has regulatory functions controlled by phosphorylation. Defects in the gene encoding PHKB are the cause of glycogen storage disease type 9B, which is also known as phosphorylase kinase deficiency of liver and muscle. This disease is characterized by a mild phenotype of hepatomegaly with only slightly elevated transaminase and plasma lipids, no clinical muscle involvement, and generally is correlated with a gradual improvement with increasing age. There are four isoforms of PHKB that are produced as a result of alternative splicing events.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: D6S113E; DADB-17J1.3; DKFZp686D20235; DKFZp686N0336; FLJ31942; FLJ36550; FLJ43813; FSH; FSRG1; KIAA9001; MGC129615; MGC40413; NAT; Polycomb group RING finger protein 3; ring finger protein 3; RING finger protein 3A; RING3; unnamed protein product

          View more View less

          Gene Aliases: 2310035N15Rik; AI662857; D630042K08Rik; DONG1; E430039C14; PCGF3; RNF3; RNF3A

          View more View less

          UniProt ID: (Human) Q3KNV8, (Mouse) Q8BTQ0

          View more View less

          Entrez Gene ID: (Human) 10336, (Mouse) 69587, (Rat) 305624

          View more View less

          Function(s)
          protein binding zinc ion binding metal ion binding histone H2AK119 ubiquitin ligase activity molecular_function histone modifying enzyme
          Process(es)
          regulation of transcription from RNA polymerase II promoter random inactivation of X chromosome transcription, DNA-templated regulation of transcription, DNA-templated biological_process
          It has to be done as per old AB suggested Products section.

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          If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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