HCCS antibody (Middle Region)

Catalog No. ABIN952686

Product Details anti-HCCS Antibody

Target: HCCS (Holocytochrome C Synthase (HCCS))

Binding Specificity: AA 179-209, Middle Region

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HCCS antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Specificity: This antibody recognizes Human and Mouse HCCS / CCHL (Center).

Purification: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 179~209 amino acids from the Central region of human HCCS / CCHL

Isotype: Ig Fraction

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Preservative: Sodium azide

Precaution of Use: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

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.

Target Details for HCCS

Target: HCCS (Holocytochrome C Synthase (HCCS))

Alternative Name: HCCS / CCHL (HCCS Products)

Synonyms: hccsb antibody, id:ibd1278 antibody, wu:fb18h01 antibody, wu:fc64e12 antibody, wu:fi43e01 antibody, cchl antibody, mcops7 antibody, DDBDRAFT_0217711 antibody, DDBDRAFT_0266707 antibody, DDB_0217711 antibody, DDB_0266707 antibody, CCHL antibody, MCOPS7 antibody, RGD1563855 antibody, holocytochrome c synthase b antibody, holocytochrome c synthase antibody, cytochrome c heme-lyase antibody, cytochrome c-type heme lyase antibody, holocytochrome c synthetase antibody, hccsb antibody, hccs antibody, cchl antibody, HCCS antibody, Hccs antibody, LOC100356413 antibody

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.Synonyms: Cytochrome c-type heme lyase, Holocytochrome c-type synthase

Molecular Weight: 30602 Da

Gene ID: 3052

NCBI Accession: NP_001116080