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Anti-NF-L Mouse Monoclonal Antibody [clone: 5C12G4]

Catalog Number: (10090-644)

Supplier: Proteintech

Description: NEFL, also named as NF68 and NFL, belongs to the intermediate filament family. Neurofilaments are the 10nm intermediate filaments found specifically in neurons. They are a major component of the cell's cytoskeleton, and provide support for normal axonal radial growth. Neurofilaments usually contain three intermediate filament proteins: L, M, and H which are involved in the maintenance of neuronal caliber. The names given to the three major neurofilament subunits are based upon the apparent molecular weight of the mammalian subunits on SDS-PAGE:NF-L, 65-68kd; NF-M,145-160kd and NF-H, 200-220kd.This antibody is specific to NEFL. It has a very weak reaction to NEFM.

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Anti-MTMR2 Rabbit Polyclonal Antibody

Catalog Number: (10090-568)

Supplier: Proteintech

Description: MTMR2(myotubularin-related protein 2) is also named as KIAA1073 and belongs to the non-receptor class myotubularin subfamily, which is characterized by the presence of a phosphatase domain. It may regulate vesicular trafficking in Schwann cells and its reversible phosphorylation represents a critical mechanism for regulating the subcellular localization of MTMR2. Mtmr2 is a 73 kDa protein in its monomeric form and exist as a dimer within cells and the protein re-localizes to membranes in hypo-osmotic settings. Defects in MTMR2 are the cause of Charcot-Marie-Tooth disease type 4B1 (CMT4B1).

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Anti-NDUFA5 Rabbit Polyclonal Antibody

Catalog Number: (10090-634)

Supplier: Proteintech

Description: NDUFA5, also named as CI-13kD-B and NDUA5, belongs to the complex I NDUFA5 subunit family. It is accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which functions in the transfer of electrons from NADH to the respiratory chain. NDUFA5,an enrichment of mitochondrial protein, can be used as a mitochondrial marker protein.

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Anti-PPBP Rabbit Polyclonal Antibody

Catalog Number: (10090-616)

Supplier: Proteintech

Description: PPBP, slso named as NAP2, or β-Thromboglobulin, is a platelet-derived growth factor that belongs to the CXC chemokine family. This growth factor is a potent chemoattractant and activator of neutrophils. It has been shown to stimulate various cellular processes including DNA synthesis, mitosis, glycolysis, intracellular cAMP accumulation, prostaglandin E2 secretion, and synthesis of hyaluronic acid and sulfated glycosaminoglycan. It also stimulates the formation and secretion of plasminogen activator by synovial cells.

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Anti-MUTYH Rabbit Polyclonal Antibody

Catalog Number: (10090-662)

Supplier: Proteintech

Description: MUTYH(MutY homolog) is also named as MYH and belongs to the Nth/MutY family. The gene enconde an A/G-specific adenine DNA glycosylase that it is involved in oxidative DNA damage repair and initiates repair of A*oxoG to C*G by removing the inappropriately paired adenine base from the DNA backbone. Possesses both adenine and 2-OH-A DNA glycosylase activities. Defects in MUTYH are a cause of familial adenomatous polyposis type 2 (FAP2) and gastric cancer (GASC). It has 6 isoforms produced by alternative splicing with the molecular weight between 57 kDa and 60 kDa.

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Anti-NDOR1 Rabbit Polyclonal Antibody

Catalog Number: (10090-622)

Supplier: Proteintech

Description: Anti-NDOR1 Rabbit Polyclonal Antibody

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Anti-NAPL1 Rabbit Polyclonal Antibody

Catalog Number: (10090-612)

Supplier: Proteintech

Description: Anti-NAPL1 Rabbit Polyclonal Antibody

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Anti-TLK2 Rabbit Polyclonal Antibody

Catalog Number: (10096-044)

Supplier: Proteintech

Description: Anti-TLK2 Rabbit Polyclonal Antibody

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Anti-TIN2 Rabbit Polyclonal Antibody

Catalog Number: (10096-022)

Supplier: Proteintech

Description: Anti-TIN2 Rabbit Polyclonal Antibody

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Anti-TMC1 Rabbit Polyclonal Antibody

Catalog Number: (10096-058)

Supplier: Proteintech

Description: TMC1 belongs to the TMC family. It is required for the normal function of cochlear hair cells. Defects in TMC1 are the cause of deafness autosomal dominant type 36 (DFNA36). Defects in TMC1 are the cause of deafness autosomal recessive type 7 (DFNB7). The antibody is specific to TMC1.