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WB analysis of A2058, A375, K562, HeLa, MCF-7 cell lysate (35ug/lane) using GTX81004 Histone H2A type 1H antibody, N-term.
WB analysis of A2058, A375, K562, HeLa, MCF-7 cell lysate (35ug/lane) using GTX81004 Histone H2A type 1H antibody, N-term.
WB analysis of A2058, A375, K562, HeLa, MCF-7 cell lysate (35ug/lane) using GTX81004 Histone H2A type 1H antibody, N-term.

Histone H2A type 1H antibody, N-term

GTX81004
GeneTex
TargetH2AC12
Product group Antibodies
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Overview

  • Supplier
    GeneTex
  • Product Name
    Histone H2A type 1H antibody, N-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:1000. IHC-P: 1:50-1:100. FACS: 1:10-1:50. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Formulation
    Liquid
  • Gene ID85235
  • Target name
    H2AC12
  • Target description
    H2A clustered histone 12
  • Target synonyms
    dJ86C11.1; H2A histone family member; H2A/S; H2AFALii; H2AH; HIST1H2AH; histone cluster 1 H2A family member h; histone cluster 1, H2ah; histone H2A type 1-H; histone H2A/s
  • Protein IDQ96KK5
  • Protein Name
    Histone H2A type 1-H
  • Scientific Description
    Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2A family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the histone microcluster on chromosome 6p21.33. [provided by RefSeq, Aug 2015]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Quantitative Proteomics Identify the Possible Tumor Suppressive Role of Protease-Activated Receptor-4 in Esophageal Squamous Cell Carcinoma Cells. Wang M et al., 2019 Jul, Pathol Oncol Res
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