Holocytochrome C Synthase (HCCS) (AA 179-209), (Middle Region) antibody

Details for Product No. ABIN952686
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Antigen
Synonyms CCHL, MCOPS7, RGD1563855, hccsb, id:ibd1278, wu:fb18h01, wu:fc64e12, wu:fi43e01, cchl, mcops7, DDBDRAFT_0217711, DDBDRAFT_0266707, DDB_0217711, DDB_0266707
Epitope
AA 179-209, Middle Region
(3), (2), (2), (2), (2), (1), (1), (1)
Reactivity
Human, Mouse (Murine)
(42), (25), (15), (12)
Host
Rabbit
(35), (8)
Clonality
Polyclonal
Conjugate
Un-conjugated
(1), (1), (1), (1), (1), (1), (1), (1), (1), (1), (1)
Application
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Western Blotting (WB)
(32), (16), (13), (10), (7), (6), (6), (5), (2), (2)
Pubmed 3 references available
Catalog no. ABIN952686
Quantity 0.4 mL
Price
357.50 $   Plus shipping costs $45.00
Shipping to United States (Change)
Availability Will be delivered in 6 to 8 Business Days

Order hotline:

  • +1 404 474 4654
  • +1 888 205 9894 (TF)
Immunogen KLH conjugated synthetic peptide between 179~209 amino acids from the Central region of human HCCS / CCHL
Specificity This antibody recognizes Human and Mouse HCCS / CCHL (Center).
Purification Protein A column, followed by peptide affinity purification
Alternative Name HCCS / CCHL
Background 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.
Alternate names: Cytochrome c-type heme lyase, Holocytochrome c-type synthase
Molecular Weight 30602 Da
Gene ID 3052
NCBI Accession NP_001116080
Restrictions For Research Use only
Format Liquid
Concentration 0.25 mg/mL
Buffer PBS containing 0.09% (w/v) Sodium Azide as preservative
Preservative Sodium azide
Handling Advice Avoid repeated freezing and thawing.
Storage 4 °C/-20 °C
Storage Comment Store undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer.
Expiry Date 12 months
Background publications Prakash, Cormier, McCall et al.: "Loss of holocytochrome c-type synthetase causes the male lethality of X-linked dominant microphthalmia with linear skin defects (MLS) syndrome." in: Human molecular genetics, Vol. 11, Issue 25, pp. 3237-48, 2002 (PubMed).

Nakashima-Kamimura, Asoh, Ishibashi et al.: "MIDAS/GPP34, a nuclear gene product, regulates total mitochondrial mass in response to mitochondrial dysfunction." in: Journal of cell science, Vol. 118, Issue Pt 22, pp. 5357-67, 2005 (PubMed).

Need, Attix, McEvoy et al.: "A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB." in: Human molecular genetics, Vol. 18, Issue 23, pp. 4650-61, 2009 (PubMed).

Hosts (35), (8)
Reactivities (42), (25), (15), (12)
Applications (32), (16), (13), (10), (7), (6), (6), (5), (2), (2)
Conjugates (1), (1), (1), (1), (1), (1), (1), (1), (1), (1), (1)
Epitopes (3), (2), (2), (2), (2), (1), (1), (1)
Request Want additional data for this product?

The Independent Validation Initiative strives to provide you with high quality data. Find out more

Order hotline:

  • +1 404 474 4654
  • +1 888 205 9894 (TF)
Validation Images
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