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Anti-ACTBL1 antibody (bs-8594R)

Anti-ACTBL1 antibody (bs-8594R)

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Anti-ACTBL1 antibody

英文名称ACTBL1
中文名称卵巢、胎盘、前列腺、睾丸蛋白22抗体
别    名ACTBL1; ovary; testis-expressed protein on chromosome 22; A26C3; Actin, beta like 1; ANKRD26 like family C, member 3; ANKRD26-like family C member 3; Cancer/testis antigen family 104, member 7; CT104.7; LA16c 3G11.6; POTE 22; POTE ankyrin domain family member H; POTE ankyrin domain family, member H; POTE-22; POTE22; POTEH; POTEH_HUMAN; Prostate; Prostate, ovary, testis expressed protein on chromosome 22; protein expressed in prostate, ovary, testis, and placenta 22; protein expressed in prostate, ovary, testis, and placenta POTE14 like.

DATASHEET

Host:Rabbit

Target Protein:ACTBL1

IR:Immunogen Range:151-250/545

Clonality:Polyclonal

Isotype:IgG

Entrez Gene:23784

Swiss Prot:Q6S545

Source:KLH conjugated synthetic peptide derived from human ACTBL1/Ovary:151-250/545 

Purification:affinity purified by Protein A

Storage:0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

Background:Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Size:100ul

Concentration:1mg/ml

Applications:WB(1:500-2000)
ELISA(1:5000-10000)
IHC-P(1:100-500)
IHC-F(1:100-500)
ICC(1:100-500)
IF(1:100-500)

Cross Reactive Species:Human
.

For research use only. Not intended for diagnostic or therapeutic use.

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