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Cullin 7 Products

(Cullin 7 (CUL7))

Categories

The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009].

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Featured Cullin 7 Categories

Cullin 7 Antibodies

High quality antibodies with extensive validation data.

Recommended Cullin 7 Antibodies

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Application WB, IP, IHC (p), IF, ICC
Validations
  • (4)
Cat. No. ABIN2856935
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application ELISA, IHC, IF
Validations
  • (3)
Cat. No. ABIN7148760
Quantity 100 μg
Datasheet Datasheet
Reactivity Human, Rat
Application ELISA, IHC
Validations
  • (2)
Cat. No. ABIN7234947
Quantity 200 μL
Datasheet Datasheet

Recommended Cullin 7 ELISA Kits

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Analytical Method Quantitative Sandwich ELISA
Validations
Cat. No. ABIN6203593
Quantity 96 tests
Datasheet Datasheet

Recommended Cullin 7 Proteins

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source Wheat germ
Validations
  • (1)
Cat. No. ABIN1350773
Quantity 10 μg
Datasheet Datasheet

Latest Publications for our Cullin 7 products

Fahlbusch, Dawood, Hartner, Menendez-Castro, Nögel, Tzschoppe, Schneider, Strissel, Beckmann, Schleussner, Ruebner, Dörr, Schild, Rascher, Dötsch: "Cullin 7 and Fbxw 8 expression in trophoblastic cells is regulated via oxygen tension: implications for intrauterine growth restriction?" in: The journal of maternal-fetal & neonatal medicine, Vol. 25, Issue 11, pp. 2209-15, (2012) (PubMed).

Nelson, Glenn, Zhang, Wen, Knutson, Gouvion, Robinson, Zhou, Yang, Smith, Paulson: "Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 27, Issue 19, pp. 5163-71, (2007) (PubMed).

Arai, Kasper, Skaar, Ali, Takahashi, DeCaprio: "Targeted disruption of p185/Cul7 gene results in abnormal vascular morphogenesis." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 100, Issue 17, pp. 9855-60, (2003) (PubMed).

Dias, Dolios, Wang, Pan: "CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 99, Issue 26, pp. 16601-6, (2002) (PubMed).

Synonyms and alternative names related to Cullin 7

cullin 7 (CUL7), cullin 7 (Cul7), 2510004L20Rik, AA409809, C230011P08Rik, CUL7, cullin-7, Cullin-7, dJ20C7.5, KIAA0076, p185, p193

Protein level used designations for Cullin 7

  • cullin 7
  • CUL-7
  • cullin-7
  • cullin-7-like
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