Anti-SUGCT Antibody

$99.00$319.00

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

Clear
-$50 as credit for submitting review for primary antibody
Shipping notice:
Product will be delivered in 6 to 8 Business Days

Rabbit Anti-SUGCT Antibody (CSB-PA867183ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Dermal papilla-derived protein 13 Antibody,SuccinylCoA:glutarate-CoA transferase Antibody,SUGCT Antibody,C7orf10 Antibody, DERP13 Antibody

More alternative names for the antibody
Chromosome 7 open reading frame 10 antibody|Dermal papilla derived protein 13 antibody|DERP13 antibody|FLJ11808 antibody|Hypothetical protein LOC79783 antibody|ORF19 antibody|Russel-Silver syndrome candidate antibody|Uncharacterized protein C7orf10 antibody
Anti-C7orf10 antibody (ab69473)
Close

Recommended applications: ELISA, WB, IHC

Recommended dilution: Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-SUGCT Antibody

Catalogue No.

CSB-PA867183ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Succinate–hydroxymethylglutarate CoA-transferase protein (1-250AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

48 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:79783( Human), Omim:609187( Human), SwissProt:Q9HAC7( Human)

Protein function

Catalyzes the succinyl-CoA-dependent conversion of glutarate to glutaryl-CoA. Can use different dicarboxylic acids as CoA acceptors, the preferred ones are glutarate, succinate, adipate, and 3-hydroxymethylglutarate. .

Protein tissue specificity

Highly expressed in kidney. Intermediate expression in liver, skeletal muscle and pancreas. Little to no expression detected in other tissues examined. .

Involvement in disease

Glutaric aciduria 3 (GA3) [MIM:231690]: A metabolic disorder due to peroxisomal glutaryl-CoA oxidase deficiency and characterized by the excretion of abnormal quantities of glutaric acid but low 3-hydroxyglutaric acid. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the CaiB/BaiF CoA-transferase family.

Protein cellular localization

Mitochondrion .

Note

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

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

Reviews


There are no reviews yet.

Only logged in customers who have purchased this product may leave a review

There are no reviews for this product yet.
By submitting a review, get following benefits:

1. Receive $50 ABcoins as credit for each review.
2. First trial sample order will be fully refunded as credit.
3. Have a chance to win a $50 amazon gift card!

view database submit reviews

There is no extra validation for this product yet.
Check other extra validated antibodies below:



Welcome to AntibodyPlus!