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Thermo Fisher Scientific PEX19 Monoclonal Antibody (GT554)
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Thermo Fisher Scientific PEX19 Monoclonal Antibody (GT554)

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PEX19 단백질을 인식하는 Thermo Fisher Scientific의 단일클론 항체로, Western blot, IHC, ICC/IF, Flow Cytometry 등 다양한 응용에 적합. Human 및 Mouse 반응성. Protein G로 정제된 액상형 항체로, 장기 보관 시 -20°C에서 안정적 유지.

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마지막 업데이트 2025. 08. 05. 오전 10:10
Thermo Fisher Scientific MA517266 PEX19 Monoclonal Antibody (GT554) 100 ul pk판매 단위 pk ·
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689,200원VAT 포함 758,120원

Thermo Fisher Scientific · Thermo Fisher Scientific PEX19 Monoclonal Antibody (GT554)

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:500–1:10,000 View 3 publications
Immunohistochemistry (IHC) - View 2 publications
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000 -
Immunocytochemistry (ICC/IF) 1:100–1:1,000 -
Flow Cytometry (Flow) 1:50–1:200 -

Product Specifications

Property Description
Species Reactivity Human, Mouse
Published Species Human, Mouse
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone GT554
Immunogen Recombinant fragment containing amino acids 1–299 of PEX19
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains No preservative
Storage Conditions Store at 4°C short term; for long-term storage, store at -20°C, avoiding freeze/thaw cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2538734

Product Specific Information

  • Recommended positive controls: Jurkat, Raji, K562, THP-1, HL-60, NCI-H929, mouse liver
  • Predicted reactivity: Mouse (91%), Rat (93%), Bovine (95%)
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are essential for the assembly of functional peroxisomes.
Peroxisome biogenesis disorders (PBDs) are genetically heterogeneous autosomal recessive diseases characterized by multiple defects in peroxisome function.
Defects in this gene are a cause of Zellweger syndrome (ZWS).


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

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