Anti-UQCC2 Antibody

$99.00$319.00

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

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Rabbit Anti-UQCC2 Antibody (CSB-PA866268ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Ubiquinol-cytochrome-c reductase complex assembly factor 2 Antibody,Breast cancer-associated protein SGA-81M Antibody,Mitochondrial nucleoid factor 1 Antibody,Mitochondrial protein M19 Antibody,UQCC2 Antibody,C6orf125 Antibody,MNF1 Antibody

More alternative names for the antibody
bA6B20.2 antibody|Breast cancer-associated protein SGA-81M antibody|C6orf125 antibody|Cbp6 antibody|M19 antibody|Mitochondrial nucleoid factor 1 antibody|Mitochondrial protein M19 antibody|MNF1 antibody|RP11-6B20.2 antibody
Anti-MNF1 antibody (ab150849)
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Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-UQCC2 Antibody

Catalogue No.

CSB-PA866268ESR2HU

Reactivity

Human

Immunogen

Recombinant human Ubiquinol-cytochrome-c reductase complex assembly factor 2 protein (14-126AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

14 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:84300( Human), Omim:614461( Human), SwissProt:Q9BRT2( Human)

Protein function

Required for the assembly of the ubiquinol-cytochrome c reductase complex (mitochondrial respiratory chain complex III or cytochrome b-c1 complex). Plays a role in the modulation of respiratory chain activities such as oxygen consumption and ATP production and via its modulation of the respiratory chain activity can regulate skeletal muscle differentiation and insulin secretion by pancreatic beta-cells. Involved in cytochrome b translation and/or stability. .

Protein tissue specificity

Pancreas, skeletal muscle, kidney, liver and heart. .

Involvement in disease

Mitochondrial complex III deficiency, nuclear 7 (MC3DN7) [MIM:615824]: A form of mitochondrial complex III deficiency, a disorder of the mitochondrial respiratory chain resulting in a highly variable phenotype depending on which tissues are affected. MC3DN7 is characterized by severe intrauterine growth retardation, neonatal lactic acidosis and renal tubular dysfunction. Additional clinical features include a dysmorphic facial appearance, delayed psychomotor development, autistic features, aggressive behavior, and mild sensorineural hearing loss. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein cellular localization

Mitochondrion matrix, mitochondrion nucleoid. Mitochondrion. Mitochondrion intermembrane space . Mitochondrion matrix . Mitochondrion inner membrane . Note=Predominantly expressed in the mitochondrial inner membrane. .

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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