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ELK Biotechnology GR (phospho Ser203) rabbit pAb
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ELK Biotechnology GR (phospho Ser203) rabbit pAb

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GR 단백질의 Ser203 인산화 부위를 인식하는 rabbit polyclonal antibody. WB 및 ELISA에 적합하며, 인간 및 생쥐 시료에 반응. 세포 내 GR의 위치 및 전사 조절 연구에 유용. -20°C에서 1년 보관 가능.

판매단위
pk
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ELK Biotechnology ES5663-100UL GR (phospho Ser203) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES5663-50UL GR (phospho Ser203) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology GR (phospho Ser203) rabbit pAb

제품명

GR (phospho Ser203) rabbit pAb

제품 정보

항목 내용
Alternative Names NR3C1; GRL; Glucocorticoid receptor; GR; Nuclear receptor subfamily 3 group C member 1
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/10000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human GR around the phosphorylation site of Ser203 (AA range: 171–220)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 86 kD
Gene ID (Human) 2908
Human Swiss-Prot No. P04150
Species Reactivity Human; Mouse

세포 내 위치

  • Isoform Alpha: Cytoplasm, Nucleus, Mitochondrion, Cytoskeleton (spindle, centrosome). After ligand activation, translocates from cytoplasm to nucleus. Shows time-dependent localization with NR1D1.
  • Isoform Beta: Predominantly nuclear, with some cytoplasmic expression.
  • Isoform Alpha-B: Cytoplasm and nucleus; translocates to nucleus upon ligand activation.

Background

This gene encodes the glucocorticoid receptor (GR), which functions both as a transcription factor binding to glucocorticoid response elements in target gene promoters and as a regulator of other transcription factors. Normally located in the cytoplasm, the receptor translocates to the nucleus upon ligand binding. It plays key roles in inflammatory response, cell proliferation, and differentiation. Mutations in this gene are associated with generalized glucocorticoid resistance. Alternative splicing and multiple translation initiation sites result in several functional isoforms with diverse cytoplasm-to-nucleus trafficking patterns.

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