HCCS Polyclonal Antibody

• Background:

  Holocytochrome c synthase (HCCS) Homo sapiens The protein encoded by this gene is an enzyme that covalently links a heme group to the apoprotein of cytochrome c. Defects in this gene are a cause of microphthalmia syndromic type 7 (MCOPS7) . Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2010]

• Product Name Alternative:

  HCCS; CCHL; Cytochrome c-type heme lyase; CCHL; Holocytochrome c-type synthase

• Gene ID:

  3052

• Swiss Prot:

  P53701

• Cross Reactivity:

  Human; Mouse; Monkey

• Clonality:

  Polyclonal

• Source:

  Rabbit

• Applications:

  WB; IHC-p; IF/ICC; ELISA

• Dilution:

  Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.

• Buffer:

  Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• Molecular Weight:

  31

• Storage Conditions:

  -20°C/1 year

• Protein Weight:

  31