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ELK Biotechnology c-Kit (phospho Tyr936) rabbit pAb
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ELK Biotechnology c-Kit (phospho Tyr936) rabbit pAb

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c-Kit (phospho Tyr936) rabbit pAb는 인산화 Tyr936 부위를 인식하는 폴리클로날 항체로, WB, IHC, IF, ELISA에 적합합니다. 인간 및 생쥐 시료에서 사용 가능하며, 세포막 및 세포질 내 단백질 검출에 유용합니다. -20°C에서 1년 보관 가능합니다.

카탈로그번호
ES6021-xxxxx (2개 옵션)
판매단위
pk
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2개 옵션
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ELK Biotechnology ES6021-100UL c-Kit (phospho Tyr936) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES6021-50UL c-Kit (phospho Tyr936) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology c-Kit (phospho Tyr936) rabbit pAb

ELK Biotechnology c-Kit (phospho Tyr936) rabbit pAb

제품 정보

항목 내용
Product name c-Kit (phospho Tyr936) rabbit pAb
Alternative Names KIT; SCFR; Mast/stem cell growth factor receptor Kit; SCFR; Piebald trait protein; PBT; Proto-oncogene c-Kit; Tyrosine-protein kinase Kit; p145 c-kit; v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog; CD antigen CD117
Applications WB; IHC; IF; ELISA
Recommended Dilutions Western Blot: 1/500–1/2000
Immunohistochemistry: 1/100–1/300
ELISA: 1/5000
Not yet tested in other applications
Immunogen The antiserum was produced against synthesized peptide derived from human KIT around the phosphorylation site of Tyr936. AA range: 906–955
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 145 kD
Gene ID (Human) 3815
Human Swiss-Prot No. P10721
Cellular Localization [Isoform 1]: Cell membrane; Single-pass type I membrane protein.
[Isoform 2]: Cell membrane; Single-pass type I membrane protein.
[Isoform 3]: Cytoplasm. Detected in the cytoplasm of spermatozoa, especially in the equatorial and subacrosomal region of the sperm head.
Species Reactivity Human; Mouse

Background

This gene encodes the human homolog of the proto-oncogene c-kit, first identified as the cellular homolog of the feline sarcoma viral oncogene v-kit. The protein is a type 3 transmembrane receptor for MGF (mast cell growth factor, also known as stem cell factor).
Mutations in this gene are associated with gastrointestinal stromal tumors, mast cell disease, acute myelogenous leukemia, and piebaldism.
Multiple transcript variants encoding different isoforms have been found for this gene.
[Provided by RefSeq, Jul 2008]

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