ELK Biotechnology STRUM rabbit pAb
상품 옵션 정보 | ||||||
---|---|---|---|---|---|---|
카탈로그 번호 | 설명 | 상태 | 단위 | 가격 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
ES12895-100UL | ELK Biotechnology ES12895-100UL STRUM rabbit pAb, 100UL pk | 재고문의 | pk | 469,000원 | 515,900원 | |
ES12895-50UL | ELK Biotechnology ES12895-50UL STRUM rabbit pAb, 50UL pk | 재고문의 | pk | 320,000원 | 352,000원 |
다른 상품 둘러보기
Product name: | STRUM rabbit pAb |
Applications: | WB;IHC |
Recommended Dilutions: | WB 1:500-2000;IHC-p 1:50-300 |
Immunogen: | Synthesized peptide derived from human STRUM AA range: 515-565 |
Storage: | Rabbit |
Storage: | -20°C/1 year |
Clonality: | Polyclonal |
Isotype: | IgG |
Concentration: | 1 mg/ml |
GeneID(Human): | 9897 |
Human Swiss-Prot No: | Q12768 |
Cellular localization: | Cytoplasm, cytosol . Endoplasmic reticulum . Early endosome . Colocalizes with SYP/synaptophysin in the external molecular layer of the dentate gyrus and in motoneurons of the ventral horn of spinal cord. . |
Background: | This gene encodes a 134 kDa protein named strumpellin that is predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain. This ubiquitously expressed gene has its highest expression in skeletal muscle. The protein is named for Strumpell disease; a form of hereditary spastic paraplegia (HSP). Spastic paraplegias are a diverse group of disorders in which the autosomal dominant forms are characterized by progressive, lower extremity spasticity caused by axonal degeneration in the terminal portions of the longest descending and ascending corticospinal tracts. More than 30 loci (SPG1-33) have been implicated in hereditary spastic paraplegia diseases. [provided by RefSeq, Aug 2009], |
Species Reactivity: | Human; Mouse |
배송/결제/교환/반품 안내
배송 정보
기본 배송비 |
| 교환/반품 배송비 |
|
---|---|---|---|
착불 배송비 |
| ||
교환/반품 배송비 |
|
결제 및 환불 안내
결제 방법 |
|
---|---|
취소 |
|
반품 |
|
환급 |
|
교환 및 반품 접수
교환 및 반품 접수 기한 |
|
---|---|
교환 및 반품 접수가 가능한 경우 |
|
교환 및 반품 접수가 불가능한 경우 |
|
교환 및 반품 신청
교환 절차 |
|
---|---|
반품 절차 |
|
문의 0
로그인 후 문의를 할 수 있습니다.