ATP2A1 Antibody, Biotin conjugated

說明書

中文名稱：

ATP2A1兔多克隆抗體, Biotin偶聯
貨號：

CSB-PA002332LD01HU
規格：

￥880
其他：

產品詳情
產品評價
相關產品
靶點詳情

產品詳情

產品名稱：

Rabbit anti-Homo sapiens (Human) ATP2A1 Polyclonal antibody
Uniprot No.：

O14983
基因名：

ATP2A1
別名：

fast twitch skeletal muscle isoform antibody; AT2A1_HUMAN antibody; ATP2A antibody; ATP2A1 antibody; ATPase Ca++ transporting cardiac muscle fast twitch 1 antibody; ATPase Ca++ transporting fast twitch 1 antibody; ATPase; Ca(2+)-transporting fast twitch 1 antibody; Calcium pump 1 antibody; Calcium transporting ATPase sarcoplasmic reticulum type fast twitch skeletal muscle isoform antibody; Calcium-transporting ATPase sarcoplasmic reticulum type antibody; EC 3.6.3.8 antibody; Endoplasmic reticulum class 1/2 Ca(2+) ATPase antibody; Fast skeletal muscle SR calcium ATPase antibody; OTTHUMP00000162561 antibody; OTTHUMP00000162562 antibody; Sarcoendoplasmic reticulum calcium ATPase antibody; Sarcoplasmic reticulum Ca(2+)-ATPase 1 antibody; Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 antibody; SERCA 1 antibody; SERCA1 antibody; SERCA1 truncated isoform; included antibody; SR Ca(2+) ATPase 1 antibody; SR Ca(2+)-ATPase 1 antibody
宿主：

Rabbit
反應種屬：

Human
免疫原：

Recombinant Human Sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein (384-579AA)
免疫原種屬：

Homo sapiens (Human)
標記方式：

Biotin
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

>95%, Protein G purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
產品提供形式：

Liquid
應用范圍：

ELISA
Protocols：

ELISA Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
貨期：

Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

功能：

Key regulator of striated muscle performance by acting as the major Ca(2+) ATPase responsible for the reuptake of cytosolic Ca(2+) into the sarcoplasmic reticulum. Catalyzes the hydrolysis of ATP coupled with the translocation of calcium from the cytosol to the sarcoplasmic reticulum lumen. Contributes to calcium sequestration involved in muscular excitation/contraction.
基因功能參考文獻：
1. Study demonstrated that (a) the distribution and the expression levels of total SERCA1 and SERCA2, the activity of SR Ca2+ ATPase, and the oligomerization of SERCA1 are similar in patients with myotonic dystrophy 1, myotonic dystrophy 2, hypothyroid myopathy and control subjects; and (b) SERCA1b is expressed in patients with myotonic dystrophy, mainly in myotonic dystrophy 2 muscles. PMID: 27133661
2. These results suggest that sAnk1 interacts with SLN both directly and in complex with SERCA1 and reduces SLN's inhibitory effect on SERCA1 activity. PMID: 28487373
3. CAPN3 deficiency leads to degradation of SERCA proteins and Ca2+ dysregulation in the skeletal muscle. PMID: 27055500
4. The sphingolipid sphingosine increases the [Ca(2+)]i by inhibiting the sarco(endo)plasmic reticulum Ca(2+)-ATPase (SERCA), in a similar manner to thapsigargin (Tg), a specific inhibitor of this Ca(2+) pump. PMID: 27033604
5. Thus the human SERCA1b has a different expression pattern from that of rodents and it is associated with DM2. PMID: 25487304
6. Formalin evokes calcium transients from the endoplasmatic reticulum via SERCA1-dependent, TRPA1-independent mechanism that may underlie formaldehyde-induced pan-neuronal excitation and subsequent inflammation. PMID: 25875358
7. We conclude that PLB C-terminal residues are critical for localization, oligomerization, and regulatory function. In particular, the PLB C terminus is an important determinant of the quaternary structure of the SERCA regulatory complex. PMID: 25074938
8. Aberrant splicing of SERCA1 may alter intracellular Ca(2+) signalling in myotonic dystrophy 1 and 2 myotubes. The differing dysregulation of intracellular Ca(2+) handling in DM1 and DM2 may explain their distinct sarcolemmal hyperexcitabilities. PMID: 23888875
9. We performed a detailed study of SERCA1 protein expression in muscle of patients with BD and BS, and evaluated the alternative splicing of SERCA1 in primary cultures of normal human muscle PMID: 23911890
10. These results indicate that PKC signaling is involved in the splicing of SERCA1 and provide new evidence for a link between alternative splicing and PKC signaling. PMID: 22609207
11. both topology and function of PLN are shaped by the interactions with lipids, which fine-tune the regulation of SERCA PMID: 21576492
12. Modeling of the inhibitory interaction of phospholamban with the Ca2+ ATPase. PMID: 12525698
13. regulation by sarcolipin's involvement in binding to transmembrane helices alone or in association with phospholamban PMID: 12692302
14. kinetic analysis of SERCA1 and SERCA2 isoforms and the effects of mutation PMID: 12975374
15. The coexistence of SERCA1 and -2, together with complex mixtures of MyHCs in most of the fibers provide the human EOMs with a unique molecular portfolio that allows a highly specific fine-tuning regimen of contraction and relaxation. PMID: 14638697
16. The combination of these histological and immunoblot results is consistent with the hypothesis that diaphragm remodeling elicited by severe COPD is characterized by a fast-to-slow SERCA isoform transformation. PMID: 15718407
17. SERCA1 gene transfer increased fractional myocardial cell shortening (compared to LacZ) and accelerated relengthening kinetics. PMID: 15767202
18. We suggest that aberrant splicing of SERCA1 mRNAs might contribute to impaired Ca2+ homeostasis in DM1 muscle PMID: 15972723
19. The maximal turnover rates of the ATPase activity for SPCA1 isoforms were 4.7-6.4-fold lower than that of SERCA1a (lowest for the shortest SPCA1a isoform). PMID: 16192278
20. SERCA1, 2, and 3 sensitivity to thapsigargin is dependent on a phenylalanine 256 to valine mutation PMID: 16410239
21. a functional abnormality in SERCA1 may have a role in inferior oblique overaction, an ocular motor disorder PMID: 16642550
22. Preload stimulates SERCA expression. BNP antagonizes this mechanism. Inhibition of cGMP-dependent protein kinase restored preload-dependent SERCA upregulation in the presence of recombinant human BNP. PMID: 16754798
23. Despite similar total calcium contents, lower SERCA and PMCA activities were found in sacs associated with hydrocele compared to those associated with undescended testis suggest a difference among the levels of cytosolic calcium. PMID: 16933204
24. Our studies point to an important regulation of SERCA1b expression at the protein level and hints to a role in the growth of the developing muscle. PMID: 17010426
25. Overexpression of the CUG repeat expansion of DMPK mRNA resulted in exclusion of exon 22 of SERCA1. PMID: 17728322
26. Ca (2+) binding to Site I of SERCA1a in fact slightly reduces Trp fluorescence, and consequently that the rise in this fluorescence generally observed when two Ca (2+) ions bind to WT SERCA1a mainly reflects Ca (2+) binding at Site II of SERCA1a. PMID: 18947188
27. the increase in mechanical efficiency of cycling occurring during first weeks of endurance training may be due to down-regulation of SERCA pumps PMID: 18953100
28. The truncated variant of the sarcoendoplasmic reticulum Ca(2+)-ATPase 1 (S1T) amplifies endoplasmic reticulum stress through the PERK-eIF2alpha-ATF4-CHOP pathway. PMID: 19061639
29. Differential SERCA1a S-nitrosylation and SERCA1a/2a co-expression in subsets of slow myofibers should be considered as signs of an altered cytosolic Ca(2+) homeostasis following chronic muscle disuse PMID: 19644701
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相關疾病：

Brody myopathy (BRM)
亞細胞定位：

Endoplasmic reticulum membrane; Multi-pass membrane protein. Sarcoplasmic reticulum membrane; Multi-pass membrane protein.
蛋白家族：

Cation transport ATPase (P-type) (TC 3.A.3) family, Type IIA subfamily
組織特異性：

Skeletal muscle, fast twitch muscle (type II) fibers.
數據庫鏈接：

HGNC: 811

OMIM: 108730

KEGG: hsa:487

STRING: 9606.ENSP00000349595

UniGene: Hs.657344

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