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Thermo Fisher Scientific JAKMIP2 Polyclonal Antibody
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Thermo Fisher Scientific JAKMIP2 Polyclonal Antibody

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Rabbit polyclonal antibody targeting human JAKMIP2 for ICC/IF applications. Recombinant protein immunogen, antigen affinity purified, liquid form with 0.2 mg/mL concentration. Suitable for research use only, stored at 4°C short term or -20°C long term.

카탈로그번호
PA566740
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오후 05:22
Thermo Fisher Scientific PA566740 JAKMIP2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
791,800원VAT 포함 870,980원

Thermo Fisher Scientific · Thermo Fisher Scientific JAKMIP2 Polyclonal Antibody

Applications

  • Immunocytochemistry (ICC/IF)
    Tested Dilution: 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant Human JAKMIP2. Recombinant protein control fragment (Product #RP-107396)
Conjugate Unconjugated
Form Liquid
Concentration 0.2 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_2664336

Product Specific Information

Immunogen sequence:
RETEKQCKPLL ERNKCLAKRN DELMVSLQRM EEKLKAVTKE NSEMREKITS HPPLKKLKSL NDLDQANEEQ

Highest antigen sequence identity to the following orthologs:

  • Mouse: 100%
  • Rat: 99%

Target Information

JAKMIP2 (Janus kinase and microtubule-interacting protein 2), also known as NECC1 (neuroendocrine long coiled-coil protein 1), CTCL tumor antigen HD-CL-04, JAMIP2, or KIAA0555, is an 810 amino acid protein belonging to the JAKMIP family.
Localizes to the Golgi apparatus and is highly expressed in the brain, with moderate expression in thymus, spleen, and lung.
Exists as three alternatively spliced isoforms. The gene encoding JAKMIP2 maps to human chromosome 5q32 and mouse chromosome 18 B3.
Chromosome 5 contains 181 million base pairs and comprises nearly 6% of the human genome.
Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

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

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