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Thermo Fisher Scientific SLC25A13 Polyclonal Antibody
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Thermo Fisher Scientific SLC25A13 Polyclonal Antibody

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SLC25A13 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체. Western blot과 IHC(P)에서 검증됨. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol 버퍼에 보관. 인간, 마우스, 랫트 반응성.

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마지막 업데이트 2025. 08. 05. 오후 04:51
Thermo Fisher Scientific PA576838 SLC25A13 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC25A13 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant full length Human SLC25A13
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2720565

Product Specific Information

The antibody was affinity-purified from rabbit antiserum using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

Citrin, also known as SLC25A13 (Solute carrier family 25 member 13), ARALAR2, or CTLN2, is a 675 amino acid multi-pass mitochondrial inner membrane protein. It is expressed in liver, pancreas, kidney, brain, heart, and placenta. Citrin functions as a calcium-dependent glutamate and aspartate carrier involved in the urea cycle.
It belongs to the mitochondrial carrier family, containing three Solcar repeats and four EF-hand domains for calcium binding.
Mutations in the SLC25A13 gene cause citrullinemia type 2 (CTLN2) and neonatal intrahepatic cholestasis due to citrin deficiency (NICCD).
CTLN2 is an autosomal recessive urea cycle disorder characterized by neuropsychiatric symptoms such as memory loss, seizures, and coma. NICCD manifests in infancy with low birth weight, reduced bile flow, growth retardation, and hepatic fibrosis.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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