Anti-DNAJC19 Antibody

$99.00$319.00

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

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Rabbit Anti-DNAJC19 Antibody (CSB-PA853400ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Mitochondrial import inner membrane translocase subunit TIM14 Antibody,DnaJ homolog subfamily C member 19 Antibody,DNAJC19 Antibody,TIM14 Antibody,TIMM14 Antibody

More alternative names for the antibody
DnaJ (Hsp40) homolog, subfamily C, member 19 antibody|DnaJ homolog subfamily C member 19 antibody|DNAJC19 antibody|homolog of yeast TIM14 antibody|Mitochondrial import inner membrane translocase subunit TIM14 antibody|PAM18 antibody|TIM 14 antibody|TIM14 antibody|TIM14_HUMAN antibody|TIMM 14 antibody|TIMM14 antibody|translocase of the inner mitochondrial membrane 14 antibody|Translocase of the inner mitochondrial membrane 14, yeast homolog of antibody
Anti-DNAJC19 antibody (ab70092)
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Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-DNAJC19 Antibody

Catalogue No.

CSB-PA853400ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Mitochondrial import inner membrane translocase subunit TIM14 protein (1-116AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

12 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:131118( Human), Entrez Gene:100503724( Mouse), Entrez Gene:67713( Mouse), Omim:608977( Human), SwissProt:Q96DA6( Human), SwissProt:Q9CQV7( Mouse), Unigene:230601( Human), Unigene:274266( Mouse), Unigene:389927( Mouse)

Protein function

Probable component of the PAM complex, a complex required for the translocation of transit peptide-containing proteins from the inner membrane into the mitochondrial matrix in an ATP-dependent manner. May act as a co-chaperone that stimulate the ATP-dependent activity (By similarity). .

Protein tissue specificity

Ubiquitously expressed.

Involvement in disease

3-methylglutaconic aciduria 5 (MGA5) [MIM:610198]: An autosomal recessive disorder characterized by early-onset dilated cardiomyopathy, growth failure, cerebellar ataxia causing significant motor delays, testicular dysgenesis, growth failure and significant increases in urine organic acids, particularly 3-methylglutaconic acid and 3-methylglutaric acid. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the TIM14 family.

Protein cellular localization

Mitochondrion inner membrane ; Single-pass membrane protein .

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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