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Thermo Fisher Scientific PLP1 Monoclonal Antibody (plpc1)
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Thermo Fisher Scientific PLP1 Monoclonal Antibody (plpc1)

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PLP1 단백질을 인식하는 Mouse Monoclonal Antibody로 다양한 포유류 종에 반응. WB, IHC, ICC 등 다중 응용 가능. 단백질 G로 정제된 고순도 항체로 1 mg/mL 농도. 연구용으로만 사용.

판매단위
pk
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마지막 업데이트 2025. 08. 01. 오전 08:09
Thermo Fisher Scientific MA180034 PLP1 Monoclonal Antibody (plpc1) 100 ug pk판매 단위 pk ·
재고 확인 필요
737,100원VAT 포함 810,810원

Thermo Fisher Scientific · Thermo Fisher Scientific PLP1 Monoclonal Antibody (plpc1)

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 1:1,000 View 1 publication
Immunohistochemistry (IHC) - View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent -
Immunohistochemistry (Frozen) (IHC (F)) Assay-dependent View 1 publication
Immunocytochemistry (ICC/IF) 1:100 View 1 publication
Flow Cytometry (Flow) Assay-dependent -

Product Specifications

Specification Description
Species Reactivity Bovine, Dog, Human, Mouse, Non-human primate, Rat
Published Species Mouse, Rat
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone plpc1
Immunogen Synthetic peptide GRGTKF corresponding to C terminal region of myelin proteolipid protein
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains <0.1% sodium azide
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_2299793

Product Specific Information

Predicted to react with all mammals based on sequence homology.
Mouse anti-myelin proteolipid protein antibody, clone plpc1 recognizes myelin proteolipid protein (PLP) in many mammalian species (Stoffel et al. 1985).


Target Information

PLP1 is a transmembrane proteolipid protein that is the predominant myelin protein present in the central nervous system.
It plays roles in the compaction, stabilization, and maintenance of myelin sheaths, as well as in oligodendrocyte development and axonal survival.
Mutations in this gene cause X-linked Pelizaeus-Merzbacher disease and spastic paraplegia type 2.
Alternatively spliced transcript variants encoding distinct isoforms or having different 5` UTRs have been identified for this gene.


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

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