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ELK Biotechnology Vasohibin rabbit pAb
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ELK Biotechnology Vasohibin rabbit pAb

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인간 VASH1 유래 펩타이드로 제작된 Vasohibin 토끼 폴리클로날 항체. WB 및 ELISA에 적합하며, 세포질 및 분비 단백질 검출에 활용. 혈관신생 억제 관련 연구에 유용. -20°C에서 1년 보관 가능.

카탈로그번호
ES3685-xxxxx (2개 옵션)
판매단위
pk
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2개 옵션
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ELK Biotechnology ES3685-100UL Vasohibin rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES3685-50UL Vasohibin rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Vasohibin rabbit pAb

Vasohibin rabbit pAb

제품 정보

항목 내용
Product name Vasohibin rabbit pAb
Alternative Names VASH1; KIAA1036; VASH; Vasohibin-1
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/40000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human VASH1 (AA range: 261–310)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 40 kDa
GeneID (Human) 22846
Human Swiss-Prot No Q7L8A9
Species Reactivity Human; Mouse; Rat
Cellular Localization Cytoplasm and secreted. Mainly localizes in cytoplasm (PubMed:27879017). Some fraction is secreted via a non-canonical secretion system; interaction with SVBP promotes secretion (PubMed:27879017).

Background

  • Function: Angiogenesis inhibitor that suppresses migration, proliferation, and network formation by endothelial cells. Inhibits tumor growth and angiogenesis without affecting smooth muscle cells, fibroblasts, or cancer cell proliferation in vitro.
  • Mechanism: Acts in an autocrine manner; inhibits artery neointimal formation and macrophage infiltration. Exhibits heparin-binding activity.
  • Induction: By VEGF.
  • Post-Translational Modifications (PTM): Exists as multiple processed forms (42, 36, 32, 27 kDa). The 42 kDa form is secreted, while the 36 kDa form accumulates intracellularly.
  • Similarity: Belongs to the vasohibin family.
  • Tissue Specificity: Preferentially expressed in endothelial cells; highly expressed in fetal organs, brain, and placenta; lower expression in heart and kidney; strongly detected in microvascular endothelial cells of atherosclerotic lesions.

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