HCCS antibody (AA 1-268)

Catalog No. ABIN6141652

Product Details anti-HCCS Antibody

Target: HCCS (Holocytochrome C Synthase (HCCS))

Binding Specificity: AA 1-268

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HCCS antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Sequence: MGLSPSAPAV AVQASNASAS PPSGCPMHEG KMKGCPVNTE PSGPTCEKKT YSVPAHQERA YEYVECPIRG TAAENKENLD PSNLMPPPNQ TPAPDQPFAL STVREESSIP RADSEKKWVY PSEQMFWNAM LKKGWKWKDE DISQKDMYNI IRIHNQNNEQ AWKEILKWEA LHAAECPCGP SLIRFGGKAK EYSPRARIRS WMGYELPFDR HDWIINRCGT EVRYVIDYYD GGEVNKDYQF TILDVRPALD SLSAVWDRMK VAWWRWTS

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-268 of human HCCS (NP_005324.3).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:100

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for HCCS

Target: HCCS (Holocytochrome C Synthase (HCCS))

Alternative Name: HCCS (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.,HCCS,CCHL,LSDMCA1,MCOPS7,MLS,LDB3,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Cytochromes,Mitochondrial markers,Lipid Metabolism,Cytochromes,Lipases,Cardiovascular,Lipids,HCCS

Molecular Weight: 30 kDa

Gene ID: 3052

UniProt: P53701