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ELK Biotechnology WAVE1 (phospho Tyr125) rabbit pAb
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ELK Biotechnology WAVE1 (phospho Tyr125) rabbit pAb

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WAVE1 (phospho Tyr125) rabbit pAb는 인간, 마우스, 랫트 시료에서 인산화된 WAVE1 단백질을 검출하는 폴리클로날 항체입니다. WB, IHC, IF, ELISA에 적합하며 세포골격 및 세포접착 관련 연구에 유용합니다. -20°C에서 1년간 안정적으로 보관 가능합니다.

카탈로그번호
ES7911-xxxxx (2개 옵션)
판매단위
pk
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ELK Biotechnology ES7911-100UL WAVE1 (phospho Tyr125) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES7911-50UL WAVE1 (phospho Tyr125) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology WAVE1 (phospho Tyr125) rabbit pAb

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WAVE1 (phospho Tyr125) rabbit pAb

제품 정보

항목 내용
Alternative Names WASF1; KIAA0269; SCAR1; WAVE1; Wiskott-Aldrich syndrome protein family member 1; WASP family protein member 1; Protein WAVE-1; Verprolin homology domain-containing protein 1
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
Immunohistochemistry: 1/100 - 1/300
Immunofluorescence: 1/200 - 1/1000
ELISA: 1/5000
Not yet tested in other applications
Immunogen Synthesized peptide derived from human WAVE1 around the phosphorylation site of Tyr125 (AA range: 91-140)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 70 kDa
Gene ID (Human) 8936
Human Swiss-Prot No. Q92558
Species Reactivity Human; Mouse; Rat

세포 내 위치 (Cellular Localization)

Cytoplasm, cytoskeleton; Cell junction, synapse; Cell junction, focal adhesion.
Dot-like pattern in cytoplasm, concentrated in Rac-regulated membrane-ruffling areas (PubMed:9889097).
Partial translocation to focal adhesion sites may be mediated by interaction with SORBS2 (PubMed:18559503).
In neurons, colocalizes with activated NTRK2 after BDNF addition in endocytic sites through association with TMEM108 (By similarity).

배경 (Background)

The WAVE1 protein, a member of the Wiskott-Aldrich syndrome protein (WASP) family, plays a critical role downstream of Rac, a Rho-family small GTPase, in regulating the actin cytoskeleton required for membrane ruffling.
It associates with the actin nucleation core Arp2/3 complex to enhance actin polymerization in vitro.
Wiskott-Aldrich syndrome is an immune system disorder likely caused by defects in actin cytoskeleton regulation.
Multiple alternatively spliced transcript variants encoding the same protein have been identified (RefSeq, Jul 2008).

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