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Thermo Fisher Scientific Spastin Polyclonal Antibody
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Thermo Fisher Scientific Spastin Polyclonal Antibody

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Rabbit polyclonal antibody targeting human Spastin protein. Validated for Western blot applications. High specificity with multiple species homology. Supplied as liquid form, affinity purified, stored at -20°C. For research use only.

판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 07:22
Thermo Fisher Scientific PA544807 Spastin Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific Spastin Polyclonal Antibody

Thermo Fisher Scientific Spastin Polyclonal Antibody

Applications


Product Specifications

항목 내용
Species Reactivity Human
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide directed towards the middle region of human SPAST
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS with 2% sucrose
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2576767

Product Specific Information

  • Peptide sequence:
    RVLVMGATNR PQELDEAVLR RFIKRVYVSL PNEETRLLLL KNLLCKQGSP

  • Sequence homology:
    Cow: 100%
    Dog: 100%
    Goat: 93%
    Guinea Pig: 100%
    Horse: 100%
    Human: 100%
    Mouse: 100%
    Rabbit: 100%
    Rat: 100%
    Zebrafish: 100%


Target Information

This gene encodes a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this family share an ATPase domain and are involved in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis.
The encoded ATPase may participate in the assembly or function of nuclear protein complexes. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants have been described but their full-length sequences have not been determined.
Mutations in this gene cause the most frequent form of autosomal dominant spastic paraplegia 4.


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

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