CHD2 rabbit pAb

CAT:
855-ES9537-01
Size:
50 µL
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
CHD2 rabbit pAb - image 1

CHD2 rabbit pAb

  • Background:

    The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • Description:

    The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008],
  • Gene ID:

    1106
  • UniProt:

    O14647
  • Cellular Locus:

    Nucleus. Binds to myogenic gene promoters..
  • Host:

    Rabbit
  • Species Reactivity:

    Human, Rat, Mouse,
  • Reactivity:

    Human; Rat; Mouse
  • Immunogen:

    Synthesized peptide derived from part region of human protein
  • Clonality:

    Polyclonal
  • Isotype:

    IgG
  • Source:

    Rabbit
  • Applications:

    WB, ELISA
  • Validated Applications:

    WB, ELISA
  • Stability:

    -20°C/1 year
  • Concentration:

    1 mg/mL
  • Dilution:

    WB 1:500-2000 ELISA 1:5000-20000
  • Molecular Weight:

    201kD
  • Storage Conditions:

    PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.
  • Observed Molecular Weight:

    201 kD
  • Subcellular Location:

    Nucleus . Binds to myogenic gene promoters. .
  • Gene ID (Human):

    1106
  • SwissProt (Human):

    O14647