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Thermo Fisher Scientific PLOD2 Monoclonal Antibody (OTI7G5), TrueMAB
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Thermo Fisher Scientific PLOD2 Monoclonal Antibody (OTI7G5), TrueMAB

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PLOD2 단백질을 인식하는 Mouse monoclonal 항체로 Western Blot과 IHC(Paraffin)에 적합합니다. Human 시료에 반응하며, 동결건조 형태로 제공됩니다. 고순도 친화 크로마토그래피 정제, 보존제 무첨가, -20°C 보관 권장.

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마지막 업데이트 2025. 08. 04. 오전 07:10
Thermo Fisher Scientific CF803225 PLOD2 Monoclonal Antibody (OTI7G5), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific PLOD2 Monoclonal Antibody (OTI7G5), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:150

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone OTI7G5
Immunogen Human recombinant protein fragment corresponding to amino acids 359–640 of human PLOD2 produced in E. coli.
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL of distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, it is recommended to perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).

Target Information

The PLOD2 gene encodes a membrane-bound homodimeric enzyme localized to the cisternae of the rough endoplasmic reticulum.
This enzyme, requiring iron and ascorbate as cofactors, catalyzes the hydroxylation of lysyl residues in collagen-like peptides.
The hydroxylysyl groups serve as attachment sites for carbohydrates in collagen, contributing to the stability of intermolecular crosslinks.
Deficiency in lysyl hydroxylase activity has been linked to Ehlers-Danlos syndrome type VIB, and mutations in this gene are associated with Bruck syndrome.
Alternative splicing results in multiple transcript variants encoding different isoforms.


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

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