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Thermo Fisher Scientific VAMP A/B Polyclonal Antibody
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Thermo Fisher Scientific VAMP A/B Polyclonal Antibody

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VAMP A/B 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, WB 및 IHC 등 다양한 응용 가능. 인간, 마우스, 랫트 반응성. 동결건조 형태로 장기 보관 시 -20°C에서 안정적. 연구용으로만 사용.

카탈로그번호
OSV00014W-100UL
판매단위
pk
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마지막 업데이트 2025. 07. 31. 오후 04:17
Thermo Fisher Scientific OSV00014W-100UL VAMP A/B Polyclonal Antibody 100 ul pk판매 단위 pk ·
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563,100원VAT 포함 619,410원

Thermo Fisher Scientific · Thermo Fisher Scientific VAMP A/B Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 1:2,000–1:3,000 -
Immunohistochemistry (Paraffin) (IHC (P)) Assay-dependent -
Immunohistochemistry - Free Floating (IHC (Free)) 1:2,000 -
Miscellaneous PubMed (Misc) - View 1 publication

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Published Species Not Applicable
Host / Isotype Rabbit / Ig
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide from amino acid region 50–100 of human VAMPB conjugated to blue carrier protein was used as the antigen.
Conjugate Unconjugated
Form Lyophilized
Concentration Not Determined
Storage Buffer Whole serum
Contains No preservative
Storage Conditions Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles. Glycerol (1:1) may be added for added stability.
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
  • The peptide is homologous in many species including human, rat, mouse, zebrafish, bovine, xenopus, and chicken.
  • Specificity: VAMP A and B.

Target Information

VAPA/VAPB may play a role in vesicle trafficking. Present in the plasma membrane and intracellular vesicles. Interacts with VAMP1 and VAMP2.

Subunit: Homodimer and heterodimer with VAPA
Subcellular Location: Cell membrane; Single-pass type IV membrane protein. Intracytoplasmic membrane; Single-pass type IV membrane protein.
Tissue Specificity: Ubiquitous. Isoform 1 predominates.
Disease Associations:

  • Defects in VAPB cause amyotrophic lateral sclerosis type 8 (ALS8), a neurodegenerative disorder affecting motor neurons and leading to fatal paralysis.
  • Defects in VAPB also cause proximal adult autosomal dominant spinal muscular atrophy (Finkel type), a late-onset form with a benign course.

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

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