Anti-SLC25A13 Antibody

$99.00$319.00

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

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Rabbit Anti-SLC25A13 Antibody (CSB-PA892444ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Citrin Antibody,Mitochondrial aspartate glutamate carrier 2 Antibody,Solute carrier family 25 member 13 Antibody,SLC25A13 Antibody,ARALAR2 Antibody

More alternative names for the antibody
AI785475 antibody|ARALAR2 antibody|Calcium binding mitochondrial carrier protein Aralar2 antibody|Calcium-binding mitochondrial carrier protein Aralar2 antibody|Citrin antibody|CMC2_HUMAN antibody|CTLN2 antibody|Ctrn antibody|Mitochondrial aspartate glutamate carrier 2 antibody|RGD1565889 antibody|Slc25a13 antibody|Solute carrier family 25 (citrin) member 13 antibody|Solute carrier family 25 member 13 (citrin) antibody|Solute carrier family 25 member 13 antibody
Anti-SLC25A13 antibody [EPR9968(B)] (ab156010)
Close sc-100937|sc-393303|sc-104144|sc-98624|sc-104145|

Recommended applications: ELISA, WB, IHC

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

Recommended protocols: check protocols

Name

Anti-SLC25A13 Antibody

Catalogue No.

CSB-PA892444ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Calcium-binding mitochondrial carrier protein Aralar2 protein (1-300AA)

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

74 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:10165( Human), Entrez Gene:50799( Mouse), Entrez Gene:362322( Rat), Omim:603859( Human), SwissProt:Q9UJS0( Human), SwissProt:Q9QXX4( Mouse), Unigene:489190( Human), Unigene:24513( Mouse)

Protein function

Catalyzes the calcium-dependent exchange of cytoplasmic glutamate with mitochondrial aspartate across the mitochondrial inner membrane. May have a function in the urea cycle. .

Protein tissue specificity

High levels in liver and low levels in kidney, pancreas, placenta, heart and brain. .

Involvement in disease

Citrullinemia 2 (CTLN2) [MIM:603471]: A form of citrullinemia, an autosomal recessive disease characterized primarily by elevated serum and urine citrulline levels. Ammonia intoxication is another manifestation. Citrullinemia type 2 is characterized by neuropsychiatric symptoms including abnormal behaviors, loss of memory, seizures and coma. Death can result from brain edema. Onset is sudden and usually between the ages of 20 and 50 years. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Cholestasis, neonatal intrahepatic, caused by citrin deficiency (NICCD) [MIM:605814]: A form of citrullinemia type 2 with neonatal onset, characterized by suppression of the bile flow, hepatic fibrosis, low birth weight, growth retardation, hypoproteinemia, variable liver dysfunction. Neonatal intrahepatic cholestasis due to citrin deficiency is generally not severe and symptoms disappear by one year of age with an appropriate diet. Years or even decades later, however, some individuals develop the characteristic features of citrullinemia type 2 with neuropsychiatric symptoms. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the mitochondrial carrier (TC 2.A.29) family.

Protein cellular localization

Mitochondrion inner membrane ; Multi-pass membrane protein .

Research area

All research areas>Structural Proteins>citrin
(View all antibody categories related to Structural Proteins)

Note

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Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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