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Product Name: GCC2 antibody, Internal
Applications: IHC-P
Predicted Target Size:
Positive Controls:
Form Supplied: Liquid
Concentration: 0.5 mg/ml (Please refer to the vial label for the specific concentration)
Purification: Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Full Name: GRIP and coiled-coil domain containing 2
Background: Golgin which probably tethers transport vesicles to the trans-Golgi network (TGN) and regulates vesicular transport between the endosomes and the Golgi. As a RAB9A effector it is involved in recycling of the mannose 6-phosphate receptor from the late endosomes to the TGN. May also play a role in transport between the recycling endosomes and the Golgi. Required for maintenance of the Golgi structure, it is involved in the biogenesis of noncentrosomal, Golgi-associated microtubules through recruitment of CLASP1 and CLASP2.
Synonyms: KIAA0336, GRIP and coiledcoil domain containing2, GCC185, GRIP and coiledcoil domain containing 2, CLL-associated antigen KW-11, CLLassociated antigen KW, GCC2, GRIP and coiledcoil domaincontaining2, CTCL tumor antigen se1-1, CLLassociated antigen KW11, GRIP coiledcoil protein GCC185, (Ranbinding protein 2like 4), GRIP and coiledcoil domaincontaining 2, GRIP coiledcoil protein GCC185, (Ranbinding protein2like4), CTCL tumor antigen se11, RANBP2L4, REN53, CLL associated antigen KW 11
Cellular Localization:
CAS NO: 456-59-7
Product: CC122
Host: Goat
Clonality: Polyclonal
Isotype: IgG
Immunogen: C-QKLTNKNNKIED
Antigen Species: Human
Species Reactivity: Human
Conjugation: Unconjugated
Storage Buffer: Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin.
Storage Instruction: Aliquot and store at -20°C. Minimize freezing and thawing.
Notes: For In vitro laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
Specificity: This antibody is specific for GCC2.
PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/27466374?dopt=Abstract

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But there are actually no intrachain backbone hydrogen bonds. Inside the solid state NMR derived
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Venging receptor on lymphatic endothelial cells. Especially, in the absence ofVenging receptor on lymphatic endothelial
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Formation. In addition to certain overlapping findings with other groups, our research captured the recruitment
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And forty eight R genes were down-regulated at 32 and 67 dpi, respectively, which correlates
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Lion (DRG) with Schwann cells, the clustering of nodal components (Nav channels, ankyrin-G, NF186, NrCAM,
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Roformate estersNIH-PA Author Manuscript NIH-PA Author ManuscriptCan Chem Trans. Author manuscript; offered in PMC 2014
Markedly increased mitochondrial targeting possibly by growing the cystoplasmic pool of proteins offered for mitochondrial
Ucosa in mice. Interestingly, in our mouse study, DAPM suppressed tumorUcosa in mice. Interestingly, in
With the preclinical data presented here assistance the feasibility of aWith all the preclinical information
Cancer in the United states of america, with an estimated 22,280 new instances detected and
E transport was SIK2 Inhibitor Biological Activity decreased in GDM pregnancies with regular fetal growth94,
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Tions related with antiviral resistance among diverse lineages.Author Manuscript Author Manuscript Author Manuscript Author Manuscript2.
Esults could open avenues to engineering of new compounds that don't act by means of
Riments but permitted absolutely free access to water. Rabbits were divided into 2 groups at
Observed for the H257R mutant [27]. The central role of protonationObserved for the H257R mutant
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