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Anti-COG7 Antibody (aa1-771, clone 10B2280, Azide-free) LS-C183526


Wt. Vol. Conc. Price
100 µg - 0.5 mg/ml $485
Inquire for larger quantities

LSBio (Direct) LSBio (Direct)

Alternate Forms of this Antibody

LS-C244001 APC Conjugated
LS-C244002 AP Conjugated
LS-C244003 Biotin Conjugated
LS-C244005 FITC Conjugated
LS-C244006 PE Conjugated
LS-C247503 HRP Conjugated, Azide-free

Most Popular COG7 Antibodies

Anti-COG7 Antibody (aa725-753, AP) LS-C234088
Rabbit Polyclonal (IgG) to Human COG7
Human, Mouse
Western blot, ELISA
AP Conjugated
Anti-COG7 Antibody (aa725-753, Biotin) LS-C234091
Rabbit Polyclonal (IgG) to Human COG7
Human, Mouse
Western blot, ELISA
Biotin Conjugated
Anti-COG7 Antibody (aa741-752) IHC-plus™ LS-B10299
Goat Polyclonal to Human COG7
Human, Monkey
IHC - Paraffin, Western blot, ELISA
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Mouse Monoclonal [clone 10B2280] (IgG1) to Human COG7
ICC, Western blot, ELISA (applications tested for the base form of this product only)
Unconjugated, Azide-free


Human COG7
Human (tested or 100% immunogen sequence identity)
IgG1 Monoclonal [10B2280]
Protein A purified


  • ICC
  • Western blot (1:500 - 1:1000)
  • (applications tested for the base form of this product only)

Specificity and Use

COG7 antibody was raised against recombinant protein corresponding to aa1-771 of human COG7.
Human COG7.
The applications listed have been tested for the base form of this product. Alternate forms, such as conjugated, azide-free, or ready-to-use, have not been tested.


PBS, pH 7.2. No preservative added (azide free)
May be stored at 4°C for short-term only. For long-term storage and to avoid repeated freezing and thawing, add sterile 40-50% glycerol, aliquot and store at -20°C. Aliquots are stable for at least 12 months at -20°C.
For research use only.

About COG7

P83436 NP_705831.1

COG7 Antibody, COG complex subunit 7 Antibody, CDG2E Antibody

COG7 resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.

Requested From: United States
Date Requested: 10/28/2016

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