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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 Rabbit Polyclonal Antibody로, Western blot, IHC, ICC/IF에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관됩니다. 인간 시료에 반응하며 연구용으로만 사용 가능합니다.

카탈로그번호
PA553887
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 10:37
Thermo Fisher Scientific PA553887 SLC25A13 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific SLC25A13 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC-P) 1:50–1:200
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human SLC25A13 (Product #RP-92588)
Conjugate Unconjugated
Form Liquid
Concentration 0.08 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% 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_2647401

Product Specific Information

Immunogen sequence:
KVALTKRADP AELRTIFLKY ASIEKNGEFF MSPNDFVTRY LNIFGESQPN PKTVELLSGV VDQTKDGLIS

Antigen sequence identity:

  • Mouse: 96%
  • Rat: 96%

Target Information

Citrin, also known as SLC25A13 (Solute carrier family 25 member 13), ARALAR2, or CTLN2, is a 675 amino acid multi-pass membrane protein localized to the inner mitochondrial membrane. 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.

Citrin belongs to the mitochondrial carrier family and contains three Solcar repeats and four EF-hand domains for calcium binding.
Mutations in the SLC25A13 gene are associated with citrullinemia type 2 (CTLN2) and neonatal intrahepatic cholestasis due to citrin deficiency (NICCD).

  • CTLN2: Autosomal recessive disorder causing neuropsychiatric symptoms such as memory loss, seizures, and coma.
  • NICCD: Non-lethal infant disorder characterized by 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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