Recombinant Human Myosin-8 (MYH8), partial

中文名稱：

人MYH8重組蛋白
貨號：

CSB-YP015302HU
說明書：

MSDS Datasheet
規格：
來源：

Yeast
其他：

中文名稱：

人MYH8重組蛋白
貨號：

CSB-EP015302HU
說明書：

MSDS Datasheet
規格：
來源：

E.coli
其他：

中文名稱：

人MYH8重組蛋白
貨號：

CSB-EP015302HU-B
說明書：

MSDS Datasheet
規格：
來源：

E.coli
共軛：

Avi-tag Biotinylated
E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.
其他：

中文名稱：

人MYH8重組蛋白
貨號：

CSB-BP015302HU
說明書：

MSDS Datasheet
規格：
來源：

Baculovirus
其他：

中文名稱：

人MYH8重組蛋白
貨號：

CSB-MP015302HU
說明書：

MSDS Datasheet
規格：
來源：

Mammalian cell
其他：

產品詳情
產品評價
靶點詳情

產品詳情

純度：

>85% (SDS-PAGE)
基因名：

MYH8
Uniprot No.：

P13535
別名：

DA7; Fetal myosin heavy chain; gtMHC F; MYH8; MYH8_HUMAN; MyHC peri; MyHC pn; MyHC-perinatal; Myosin 8; Myosin heavy chain 8; Myosin heavy chain; Myosin heavy chain; skeletal muscle; perinatal; Myosin; heavy chain 8; skeletal muscle; perinatal; Myosin; heavy polypeptide 8; skeletal muscle; perinatal; Myosin-8; perinatal; skeletal muscle
種屬：

Homo sapiens (Human)
蛋白長度：

Partial
蛋白標簽：

Tag?type?will?be?determined?during?the?manufacturing?process.

The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
產品提供形式：

Lyophilized powder Warning: in_array() expects parameter 2 to be array, null given in /www/web/cusabio_cn/public_html/caches/caches_template/default/content/show_product_protein.php on line 662
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
復溶：

We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
儲存條件：

Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
保質期：

The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
貨期：

Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
注意事項：

Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
Datasheet ：

Please contact us to get it.

產品評價

靶點詳情

功能：

Muscle contraction.
基因功能參考文獻：
1. There was an immediate shutdown of the MHC IIX gene after resistance exercise. Silencing of the MHC IIX gene is sustained at least 4 days after removal of the stimulus. PMID: 28508505
2. Loss-of-function variants in the MYH8 gene do not cause autosomal dominant trismus-pseudocamptodactyly syndrome. PMID: 28377322
3. a family in which two out three sibs affected with trismus pseudocamptodactyly, born from healthy nonconsanguineous parents, were heterozygous for the c.2021G > A mutation due to a possible germline mosaicism in MYH8 PMID: 20949528
4. We describe a novel heart-hand syndrome involving familial cardiac myxomas and distal arthrogryposis and demonstrate that these disorders are caused by a founder mutation in the MYH8 gene. PMID: 15282353
5. haplotype analysis revealed that this mutation has arisen independently in North American and European TPS pedigrees PMID: 17041932
6. findings broaden the phenotype associated with p.R674Q mutations and support the use of MYH8 testing in patients with a clinical diagnosis of trimus-pseudocamptodactyly syndrome PMID: 18049072
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相關疾病：

Carney complex variant (CACOV); Arthrogryposis, distal, 7 (DA7)
亞細胞定位：

Cytoplasm, myofibril. Note=Thick filaments of the myofibrils.
蛋白家族：

TRAFAC class myosin-kinesin ATPase superfamily, Myosin family
數據庫鏈接：

HGNC: 7578

OMIM: 158300

KEGG: hsa:4626

STRING: 9606.ENSP00000384330

UniGene: Hs.700484