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Thermo Fisher Scientific GDAP1 Polyclonal Antibody
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Thermo Fisher Scientific GDAP1 Polyclonal Antibody

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Rabbit polyclonal antibody against GDAP1, validated for WB, IHC(P), and ELISA. Recognizes human, mouse, and rat GDAP1. Supplied as a liquid in PBS with 50% glycerol. Ideal for research on GDAP1-related neurodegenerative pathways.

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마지막 업데이트 2025. 08. 05. 오후 05:02
Thermo Fisher Scientific PA5109760 GDAP1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific GDAP1 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
ELISA 1 µg/mL

Product Specifications

Specification Description
Species Reactivity Rat, Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1–225 of human GDAP1 (NP_001035808.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.33 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2855171

Product Specific Information

Immunogen sequence:
MRLNSTGEVP VLIHGENIIC EATQIIDYLE QTFLDERTPR LMPDKESMYY PRVQHYRELL DSLPMDAYTH GCILHPELTV DSMIPAYATT RIRSQIGNTE SELKKLAEEN PDLQEAYIAK QKRLKSKLLD HDNVKYLKKI LDELEKVLDQ VETELQRRNE ETPEEGQQPW LCGESFTLAD VSLAVTLHRL KFLGFARRNW GNGKRPNLET YYERVLKRKT FNKVL

Target Information

Glutathione S-transferases (GSTs) conjugate reduced glutathione to various hydrophobic electrophiles. GDAP1 (ganglioside-induced differentiation-associated protein 1) is a GST-like protein with an extended GST domain II and a predicted transmembrane domain, distinguishing it from typical GST family members. GDAP1 may participate in signal transduction pathways for ganglioside-induced neurite differentiation and protect myelin membranes from free-radical damage. Mutations in GDAP1 cause several forms of Charcot-Marie-Tooth disease, a hereditary peripheral neuropathy characterized by reduced nerve conduction, progressive distal muscle atrophy, and absent deep tendon reflexes.


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

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