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Rabbit Anti-HCCS Antibody (CSB-PA010165ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Cytochrome c-type heme lyase Antibody,CCHL Antibody,Holocytochrome c-type synthase Antibody,HCCS Antibody,CCHL AntibodyMore alternative names for the antibody
CCHL antibody|CCHL_HUMAN antibody|cytochrome c heme-lyase antibody|Cytochrome c-type heme lyase antibody|DKFZp779I1858 antibody|EC 18.104.22.168 antibody|Hccs antibody|Holocytochrome c synthase (cytochrome c heme lyase) antibody|Holocytochrome c synthase antibody|Holocytochrome c type synthase antibody|Holocytochrome c-type synthase antibody|MCOPS7 antibody|OTTHUMP00000022903 antibody|OTTHUMP00000022904 antibody|OTTHUMP00000022905 antibody|OTTMUSP00000021173 antibody|OTTMUSP00000021174 antibody|RGD1563855 antibody|RP23-37L2.1 antibody
Anti-HCCS antibody (ab208646)
Anti-HCCS antibody (ab208646)
Recommended applications: ELISA, WB
Recommended dilution: User optimized
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Cytochrome c-type heme lyase protein (1-268AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:3052( Human), Entrez Gene:15159( Mouse), Entrez Gene:317444( Rat), Omim:300056( Human), SwissProt:P53701( Human), SwissProt:P53702( Mouse), Unigene:211571( Human), Unigene:284033( Mouse), Unigene:162316( Rat)
|Protein function|| |
Links covalently the heme group to the apoprotein of cytochrome c. .
|Involvement in disease|| |
Linear skin defects with multiple congenital anomalies 1 (LSDMCA1) [MIM:309801]: A disorder characterized by dermal, ocular, neurological and cardiac abnormalities. LSDMCA1 main features are unilateral or bilateral microphthalmia, linear skin defects in affected females, and in utero lethality for males. Skin defects are limited to the face and neck, consisting of areas of aplastic skin that heal with age to form hyperpigmented areas. Additional features in female patients include agenesis of the corpus callosum, sclerocornea, chorioretinal abnormalities, infantile seizures, congenital heart defect, mental retardation, and diaphragmatic hernia. Microphthalmia is a disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the cytochrome c-type heme lyase family.
|Protein cellular localization|| |
Mitochondrion inner membrane . Membrane ; Lipid-anchor .
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CUSABIO BIOTECH CO.
|Product type|| |
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