CacheBy
ELK Biotechnology MYO7A rabbit pAb
원본

ELK Biotechnology MYO7A rabbit pAb

상품 한눈에 보기

MYO7A 단백질을 인식하는 토끼 다클론 항체로, WB 및 ELISA에 적합합니다. 인간 및 생쥐 시료에 반응하며, 세포질 및 세포골격에 주로 위치합니다. -20°C에서 1년 보관 가능하며, 1 mg/ml 농도로 제공됩니다.

판매단위
pk
카탈로그 보기

카탈로그

2개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
ELK Biotechnology ES9855-100UL MYO7A rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES9855-50UL MYO7A rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology MYO7A rabbit pAb

ELK Biotechnology MYO7A rabbit pAb

제품 설명

MYO7A 단백질을 인식하는 토끼 유래 다클론 항체로, Western Blot(WB) 및 ELISA 실험에 사용됩니다. 인간 및 생쥐 시료에서 반응하며, 세포질 및 세포골격 부위에 주로 발현됩니다.

제품 정보

항목 내용
Product name MYO7A rabbit pAb
Applications WB; ELISA
Recommended Dilutions WB 1:500–2000, ELISA 1:5000–20000
Immunogen Synthesized peptide derived from human protein (AA range: 830–910)
Host Rabbit
Storage -20°C, 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 243 kD
Gene ID (Human) 4647
Human Swiss-Prot No. Q13402
Species Reactivity Human; Mouse

세포 내 위치 (Cellular Localization)

Cytoplasm, cytoplasm cell cortex, cytoskeleton, cell junction, synapse.
In photoreceptor cells, mainly localized in the inner and base of outer segments as well as in the synaptic ending region (PubMed:8842737).
In retinal pigment epithelial cells, colocalizes with a subset of melanosomes, predominantly localized to stress fiber-like structures and cytoplasmic puncta (PubMed:19643958, PubMed:27331610).
Detected at the tip of cochlear hair cell stereocilia (PubMed:21709241).
The complex formed by MYO7A, USH1C, and USH1G colocalizes with F-actin (PubMed:21709241).

Background

This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor.
This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B, which are characterized by deafness, reduced vestibular function, and (in humans) retinal degeneration.
Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]

ELK Biotechnology 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.