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ELK Biotechnology SPAST rabbit pAb
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ELK Biotechnology SPAST rabbit pAb

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SPAST 단백질을 인식하는 토끼 폴리클로날 항체로, WB에 적합합니다. 인간, 마우스, 랫트 시료에 반응하며, 세포막 및 세포골격 등 다양한 세포 위치에서 발현되는 SPAST 단백질 연구에 유용합니다. -20°C에서 1년 보관 가능합니다.

판매단위
pk
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ELK Biotechnology ES12999-100UL SPAST rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES12999-50UL SPAST rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology SPAST rabbit pAb

ELK Biotechnology SPAST rabbit pAb

제품 정보

항목 내용
Product name SPAST rabbit pAb
Applications WB
Recommended Dilutions WB 1:500–2000
Immunogen Synthesized peptide derived from human SPAST (AA range: 163–213)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
GeneID (Human) 6683
Human Swiss-Prot No Q9UBP0
Species Reactivity Human, Mouse, Rat

세포 내 위치 (Cellular Localization)

Membrane; Peripheral membrane protein; Endoplasmic reticulum; Midbody; Cytoplasm (cytoskeleton, microtubule organizing center, centrosome, perinuclear region, spindle); Nucleus.
Forms an intramembrane hairpin-like structure in the membrane (PubMed:20200447).
Localization to the centrosome is independent of microtubules (PubMed:15891913).
Localizes to the midbody of dividing cells, requiring CHMP1B (PubMed:18997780).
Enriched in distal axons and branches of postmitotic neurons (PubMed:15269182).
Isoform 1: Endoplasmic reticulum membrane; Peripheral membrane protein; Nucleus membrane; Lipid droplet; Cytoplasm (cytoskeleton, endosome).

Background

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 be involved 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. (RefSeq, Jul 2008)

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