Anti-HCCS Antibody

$99.00$319.00

Reactivity: Human,Mouse
Applications: ELISA,WB
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-HCCS Antibody (CSB-PA010165ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Cytochrome c-type heme lyase Antibody,CCHL Antibody,Holocytochrome c-type synthase Antibody,HCCS Antibody,CCHL Antibody

More alternative names for the antibody
CCHL antibody|CCHL_HUMAN antibody|cytochrome c heme-lyase antibody|Cytochrome c-type heme lyase antibody|DKFZp779I1858 antibody|EC 4.4.1.17 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)
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Recommended applications: ELISA, WB

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-HCCS Antibody

Catalogue No.

CSB-PA010165ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Cytochrome c-type heme lyase protein (1-268AA)

Host

Rabbit

Applications

ELISA, WB

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

30 kDa

Purification

Antigen Affinity Purified

Storage

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 .

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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