渲染靶标:SSR
Render Timestamp:
4/4/2025, 3:56:36 PM EDT
4/4/2025, 7:56:36 PM UTC
Commit: 461ca8d8fe5b1efd4c01fc87e5b5eb592e2d154a
XML generation date: 2025-03-07 13:16:35.463
Product last modified at: 2025-03-21T23:30:09.008Z
1% for the Planet 标识
PDP - Template Name: Monoclonal Antibody
PDP - Template ID: *******c5e4b77
R Recombinant
Recombinant: Superior lot-to-lot consistency, continuous supply, and animal-free manufacturing.

TMEM106B (E7H7Z) Rabbit mAb #93334

Filter:
  • WB
  • IP
  • IF
Western Blotting Image 1: TMEM106B (E7H7Z) Rabbit mAb
Western blot analysis of extracts from various cell lines using TMEM106B (E7H7Z) Rabbit mAb (upper) or β-Actin (D6A8) Rabbit mAb #8457 (lower). Negative expression of TMEM106B protein in Raji cell extracts is consistent with the predicted expression pattern.

To Purchase # 93334

Supporting Data

REACTIVITY H M R
SENSITIVITY Endogenous
MW (kDa) 42
Source/Isotype Rabbit IgG
Application Key:
  • WB-Western Blotting 
  • IP-Immunoprecipitation 
  • IF-Immunofluorescence 
Species Cross-Reactivity Key:
  • H-Human 
  • M-Mouse 
  • R-Rat 
  • Related Products

Product Information

Product Usage Information

Application Dilution
Western Blotting 1:1000
Immunoprecipitation 1:50
Immunofluorescence (Immunocytochemistry) 1:50 - 1:200

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

Protocol

Specificity / Sensitivity

TMEM106B (E7H7Z) Rabbit mAb recognizes endogenous levels of total TMEM106B protein.

Species Reactivity:

Human, Mouse, Rat

Source / Purification

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala17 of human TMEM106B protein.

Background

Transmembrane protein 106B (TMEM106B) is a type II transmembrane protein with unknown function (1). TMEM106B was first identified as a major risk factor in genome-wide association studies in patients with frontotemporal lobar degeneration (FTLD), a neurodegenerative disorder characterized by atrophy in the frontal and temporal lobes of the brain (2). Localization of TMEM106B in late endosomal/lysosomal compartments suggests a role in regulating endo-lysosomal morphology and function (3). Endo-lysosomal dysfunction is likely a major cellular pathway that contributes to FTLD as other genetically linked FTLD genes, including C9orf72, GRN, and MAPT, converge on this cellular pathway (4).
For Research Use Only. Not For Use In Diagnostic Procedures.
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