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          • Proteins & Peptides ›
          • JPH3 Proteins

          Invitrogen

          Human JPH3 Synthetic Peptide

          View all (3) JPH3 proteins

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          Cite Human JPH3 Synthetic Peptide

          Product Details

          PEP-0764

          Applications
          Tested Dilution
          Publications

          Control (Ctrl)

          Assay-dependent
          -

          Blocking Assay (BLOCK)

          Assay-dependent
          -
          Product Specifications

          Species Reactivity

          Human

          Class

          Synthetic

          Type

          Peptide

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          200 µg/mL

          Purification

          purified

          Storage buffer

          PBS, pH 7.2, with 0.1% BSA

          Contains

          0.02% sodium azide

          Storage conditions

          -20°C

          Product Specific Information

          This peptide corresponds to 18 amino acids near the center of human JPH3.

          PEP-0764 can be used as a blocking peptide with polyclonal antibody PA5-20644.

          Target Information

          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.

          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: JP-3; Junctophilin type 3; Junctophilin-3; trinucleotide repeat containing 22; Trinucleotide repeat-containing gene 22 protein

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          Gene Aliases: CAGL237; HDL2; JP-3; JP3; JPH3; TNRC22

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          UniProt ID: (Human) Q8WXH2

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          Entrez Gene ID: (Human) 57338

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          It has to be done as per old AB suggested Products section.
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