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TMEM165 产品

(Transmembrane Protein 165 (TMEM165))

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This gene encodes a predicted transmembrane protein with a perinuclear Golgi-like distribution in fibroblasts. Mutations in this gene are associated with the autosomal recessive disorder congenital disorder of glycosylation, type IIk. Knockdown of this gene's expression causes decreased sialylation in HEK cells and suggests this gene plays a role in terminal Golgi glycosylation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012].

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Featured TMEM165 Categories

TMEM165 抗体

High quality antibodies with extensive validation data.

Recommended TMEM165 抗体

Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Application ELISA, WB, IHC, IF
Validations
  • (4)
Cat. No. ABIN7173091
Quantity 100 μg
Datasheet Datasheet
Reactivity Human
Application WB
Validations
  • (1)
Cat. No. ABIN7270956
Quantity 100 μL
Datasheet Datasheet
Reactivity Human
Application WB, FACS
Validations
  • (2)
Cat. No. ABIN651700
Quantity 400 μL
Datasheet Datasheet

Recommended TMEM165 ELISA试剂盒

Product
Reactivity
Analytical Method
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Analytical Method Quantitative Sandwich ELISA
Validations
Cat. No. ABIN6234336
Quantity 96 tests
Datasheet Datasheet

Recommended TMEM165 蛋白

Product
Reactivity
Source
Validations
Cat. No.
Quantity
Datasheet
Reactivity Human
Source Insect Cells
Validations
  • (1)
Cat. No. ABIN3107070
Quantity 1 mg
Datasheet Datasheet
Reactivity Mouse
Source Insect Cells
Validations
  • (1)
Cat. No. ABIN3134451
Quantity 1 mg
Datasheet Datasheet

Latest Publications for our TMEM165 Products

Venkat, Linstedt: "Manganese-induced trafficking and turnover of GPP130 is mediated by sortilin." in: Molecular biology of the cell, Vol. 28, Issue 19, pp. 2569-2578, (2017) (PubMed).

Foulquier, Amyere, Jaeken, Zeevaert, Schollen, Race, Bammens, Morelle, Rosnoblet, Legrand, Demaegd, Buist, Cheillan, Guffon, Morsomme, Annaert, Freeze, Van Schaftingen, Vikkula, Matthijs: "TMEM165 deficiency causes a congenital disorder of glycosylation." in: American journal of human genetics, Vol. 91, Issue 1, pp. 15-26, (2012) (PubMed).

Synonyms and alternative names related to TMEM165

transmembrane protein 165 (tmem165), transmembrane protein 165 (TMEM165), transmembrane protein 165 L homeolog (tmem165.L), transmembrane protein 165 (MCYG_08032), transmembrane protein 165 (MGYG_05482), transmembrane protein 165 (Tmem165), AV026557, CDG2K, FT27, GDT1, MGC98993, pFT27, si:ch211-278f21.2, TMPT27, Tpardl, tparl, TPARL, Tparl, wu:fc31a09, zgc:92342

Protein level used designations for TMEM165

  • TPA regulated locus
  • transmembrane protein 165
  • transmembrane protein PT27
  • transmembrane protein TPARL
  • TPA-regulated locus protein
  • transmembrane protein 164
  • transmembrane protein PFT27
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