Anti-FOXRED1 Antibody

$99.00$319.00

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

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Rabbit Anti-FOXRED1 Antibody (CSB-PA822192ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

FAD-dependent oxidoreductase domain-containing protein 1Imported Antibody,FOXRED1 Antibody

More alternative names for the antibody
FAD dependent oxidoreductase domain containing 1 antibody|FAD dependent oxidoreductase domain containing protein 1 antibody|FAD-dependent oxidoreductase domain-containing protein 1 antibody|FOXRED 1 antibody|FOXRED1 antibody|FP634 antibody|FXRD1_HUMAN antibody|H17 antibody
Anti-FOXRED1 antibody (ab94422)
Close sc-377010|sc-377264|

Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-FOXRED1 Antibody

Catalogue No.

CSB-PA822192ESR1HU

Reactivity

Human

Immunogen

Recombinant human FAD-dependent oxidoreductase domain-containing protein 1 protein (307-486AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

53 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:510097( Cow), Entrez Gene:55572( Human), Entrez Gene:235169( Mouse), Entrez Gene:315547( Rat), GenBank:NP_060017.1( Human), Omim:613622( Human), SwissProt:Q5EA45( Cow), SwissProt:Q96CU9( Human), SwissProt:Q3TQB2( Mouse), Unigene:317190( Human), Unigene:138512( Mouse)

Protein function

Required for the assembly of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) (PubMed:20858599, PubMed:25678554). Involved in mid-late stages of complex I assembly (PubMed:25678554). .

Involvement in disease

Mitochondrial complex I deficiency (MT-C1D) [MIM:252010]: A disorder of the mitochondrial respiratory chain that causes a wide range of clinical manifestations from lethal neonatal disease to adult-onset neurodegenerative disorders. Phenotypes include macrocephaly with progressive leukodystrophy, non-specific encephalopathy, cardiomyopathy, myopathy, liver disease, Leigh syndrome, Leber hereditary optic neuropathy, and some forms of Parkinson disease. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein cellular localization

Mitochondrion inner membrane ; Single-pass membrane protein . Note=According to a report, it is associated with the matrix face of the mitochondrial inner membrane and does not contain any transmembrane region. However, one transmembrane domain is clearly predicted by different methods (Probable). .

Research area

All research areas>Synthesis and Degradation>FOXRED
(View all antibody categories related to Synthesis and Degradation)

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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