HCCS rabbit pAb

• 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]

• Description:

  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],

• UniProt:

  P53701

• Swiss Prot:

  P53701

• Reactivity:

  Human; Mouse; Monkey

• Immunogen:

  The antiserum was produced against synthesized peptide derived from human Cytochrome c-type Heme Lyase. AA range:81-130

• Clonality:

  Polyclonal

• Source:

  Rabbit

• Applications:

  WB; IHC; IF; ELISA

• Concentration:

  1 mg/ml

• 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.

• Molecular Weight:

  31kD

• Storage Conditions:

  -20°C/1 year

• Observed Molecular Weight:

  31kD

• Fragment:

  IgG

• Subcellular Location:

  Mitochondrion inner membrane . Membrane ; Lipid-anchor .

• Other Product Names:

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

• Gene ID (Human):

  3052