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>   首页   >   产品   >   一抗   >   癌症   >   K1199 Antibody (C-term)   

K1199 Antibody (C-term) 精选

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - K1199 Antibody (C-term) AP10964B
    K1199 Antibody (C-term) (Cat. #AP10964b) western blot analysis in mouse spleen tissue lysates (35ug/lane).This demonstrates the K1199 antibody detected the K1199 protein (arrow).
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, E
Primary Accession Q8WUJ3
Other Accession NP_061159.1
Reactivity Human, Mouse
Predicted Rat, Bovine, Rabbit
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 152998 Da
Antigen Region 1292-1321 aa
Additional Information
Gene ID 57214
Other Names Cell migration-inducing and hyaluronan-binding protein, CEMIP, KIAA1199
Target/Specificity This K1199 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1292-1321 amino acids from the C-terminal region of human K1199.
Dilution WB~~1:1000
E~~Use at an assay dependent concentration.
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsK1199 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name CEMIP (HGNC:29213)
Function Mediates depolymerization of hyaluronic acid (HA) via the cell membrane-associated clathrin-coated pit endocytic pathway. Binds to hyaluronic acid. Hydrolyzes high molecular weight hyaluronic acid to produce an intermediate-sized product, a process that may occur through rapid vesicle endocytosis and recycling without intracytoplasmic accumulation or digestion in lysosomes. Involved in hyaluronan catabolism in the dermis of the skin and arthritic synovium. Positively regulates epithelial-mesenchymal transition (EMT), and hence tumor cell growth, invasion and cancer dissemination. In collaboration with HSPA5/BIP, promotes cancer cell migration in a calcium and PKC- dependent manner. May be involved in hearing.
Cellular Location Nucleus. Cytoplasm. Endoplasmic reticulum. Cell membrane. Membrane, clathrin-coated pit. Secreted. Note=Retained in the endoplasmic reticulum (ER) in a HSPA5/BIP-dependent manner. Colocalized with clathrin heavy chain/CLTC in clathrin-coated vesicles. Strongly detected in the cytoplasm of breast carcinoma cells, whereas poorly detected in adjacent normal epithelial cells, stromal cells, or benign breast tissues. Localized in the nucleus and cytoplasm of colon adenocarcinomas
Tissue Location Expressed in dermal and in synovial fibroblasts. Strongly expressed in gastric cancers compared with the paired normal tissues. Strongly expressed in both ductal carcinoma and invasive breast cancer cells compared with benign epithelial cells (at protein level). Strongly expressed in brain, placenta, prostate, breast, lung and testis. Expressed in fibroblasts, epithelial cells and cancer cells. In ear, it is specifically expressed in inner ear. Expressed in cochlea and vestibule tissues. Strongly expressed in gastric cancers compared with the paired normal tissues. Strongly expressed in colon adenocarcinomas compared with normal colonic mucosas. Strongly expressed in breast cancer as compared to normal breast tissue
Research Areas

BACKGROUND

May be involved in hearing.

REFERENCES

Rose, J. Phd, et al. Mol. Med. (2010) In press :
Matsuzaki, S., et al. Ann. Surg. Oncol. 16(7):2042-2051(2009)
Michishita, E., et al. Cancer Lett. 239(1):71-77(2006)
Guo, J., et al. FEBS Lett. 580(2):581-584(2006)
Abe, S., et al. Am. J. Hum. Genet. 72(1):73-82(2003)

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