DNAJC30 Antibody

• Background :

  This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.

• NCBI Gene ID :

  84277

• Swiss Prot :

  Q96LL9

• Accession Number :

  Q96LL9

• Host :

  Rabbit

• Reactivity :

  Human

• Immunogen :

  This DNAJC30 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 176-202 amino acids from the C-terminal region of human DNAJC30.

• Clonality :

  Polyclonal

• Conjugation :

  Unconjugated

• Type :

  Primary Antibodies

• Field of Research :

  Signal Transduction

• Purification :

  This antibody is purified through a protein A column, followed by peptide affinity purification.

• Concentration :

  Batch dependent

• Buffer :

  Supplied in PBS with 0.09% (W/V) sodium azide.

• Modification :

  None

• Shipping Conditions :

  Blue Ice

• Storage Conditions :

  Store at 4˚ C for three months and -20˚ C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

• Calculated Molecular Weight :

  26 kDa

• Fragment :

  Rabbit Ig

• Applications Notes :

  For WB starting dilution is: 1:1000

• Symbol :

  DNAJC30

• NCBI Official Name :

  DnaJ homolog subfamily C member 30

• NCBI Organism :

  Homo sapiens

• Background Reference 01 :

  Lamesch, P., et al. Genomics 89 (3) :307-315 (2007)

• Background Reference 02 :

  Lehner, B., et al. Genome Res. 14 (7) :1315-1323 (2004)

• Background Reference 03 :

  Merla, G., et al. Hum. Genet. 110 (5) :429-438 (2002)

• Other Product Names :

  DnaJ homolog subfamily C member 30, Williams-Beuren syndrome chromosomal region 18 protein, DNAJC30, WBSCR18

• Tested Applications :

  WB

• Protein ID :

  24212614

• Physical Properties :

  Liquid