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ELK Biotechnology p53 (Acetyl K319) rabbit pAb
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ELK Biotechnology p53 (Acetyl K319) rabbit pAb

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인간 p53 단백질의 Lys319 아세틸화 부위를 인식하는 토끼 폴리클로날 항체로, WB, IHC, IF, ELISA에 사용 가능. 고순도 IgG 형태로 제공되며, 인간·마우스·랫트 시료에 반응. 세포 내 p53 발현 및 위치 연구에 적합.

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pk
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ELK Biotechnology ES7420-100UL p53 (Acetyl K319) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7420-50UL p53 (Acetyl K319) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology p53 (Acetyl K319) rabbit pAb

ELK Biotechnology p53 (Acetyl K319) rabbit pAb

제품 정보

항목 내용
Product name p53 (Acetyl K319) rabbit pAb
Alternative Names TP53; P53; Cellular tumor antigen p53; Antigen NY-CO-13; Phosphoprotein p53; Tumor suppressor p53
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500–1/2000
Immunohistochemistry: 1/100–1/300
Immunofluorescence: 1/200–1/1000
ELISA: 1/10000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human p53 around the acetylated site of Lys317 (AA range: 283–332)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 43 kDa
Gene ID (Human) 7157
Human Swiss-Prot No. P04637
Species Reactivity Human; Mouse; Rat

Cellular Localization

Cytoplasm, Nucleus, PML body, Endoplasmic reticulum, Mitochondrion matrix, Cytoskeleton (microtubule organizing center, centrosome).
Translocates to mitochondria upon oxidative stress or mitomycin C treatment.
Isoform-specific localization:

  • Isoform 1: Predominantly nuclear, cytoplasmic when co-expressed with isoform 4
  • Isoform 2: Mainly nuclear, minor cytoplasmic staining
  • Isoform 3: Nuclear in most cells, cytoplasmic in some
  • Isoform 4: Predominantly nuclear, translocates to cytoplasm

Background

Tumor protein p53 (TP53) in Homo sapiens encodes a tumor suppressor protein with transcriptional activation, DNA binding, and oligomerization domains. It responds to various cellular stresses to regulate target genes, inducing cell cycle arrest, apoptosis, senescence, DNA repair, or metabolic changes.
Mutations in this gene are linked to numerous human cancers, including hereditary Li-Fraumeni syndrome.
Alternative splicing and promoter usage generate multiple transcript variants and isoforms, with additional isoforms arising from alternative translation initiation codons (RefSeq, Feb 2013; PMIDs: 12032546, 20937277).

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