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ELK Biotechnology FGF-13 rabbit pAb
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ELK Biotechnology FGF-13 rabbit pAb

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FGF-13 rabbit pAb는 인간, 생쥐, 랫트에서 반응하는 다클론 항체로, Western blot 및 ELISA에 적합합니다. 인간 FGF13 유래 합성 펩타이드로 면역생성되었으며, 세포 내 핵 및 세포질 위치에서 발현되는 단백질 검출에 활용됩니다. 고순도 IgG 형식으로 안정적 보관이 가능합니다.

판매단위
pk
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ELK Biotechnology ES5243-100UL FGF-13 rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES5243-50UL FGF-13 rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology FGF-13 rabbit pAb

제품명

FGF-13 rabbit pAb

기본 정보

항목 내용
Alternative Names FGF13; FHF2; Fibroblast growth factor 13; FGF-13; Fibroblast growth factor homologous factor 2; FHF-2
Applications WB; ELISA
Recommended Dilutions Western Blot: 1/500 - 1/2000
ELISA: 1/5000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human FGF13. AA range: 154-203
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 28 kD
Gene ID (Human) 2258
Human Swiss-Prot No Q92913
Species Reactivity Human; Mouse; Rat

세포 내 위치

  • Isoform 1: Nucleus
  • Isoform 2: Cytoplasm, Nucleus
  • Isoform 3: Cytoplasm, Nucleus
  • Isoform 4: Cytoplasm, Nucleus
  • Isoform 5: Cytoplasm, Nucleus
  • Cell projection: filopodium, growth cone, dendrite
  • Cell membrane: sarcolemma
  • Cytoplasm
  • Not secreted
  • Localizes to the lateral membrane and intercalated disks of myocytes

배경 정보

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in various biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion.
This gene is located on chromosome X, associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of BFLS and other X-linked mental retardation forms.
Alternative splicing at the 5' end results in several transcript variants encoding different isoforms with distinct N-termini.
[provided by RefSeq, Nov 2008]

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