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BLOC1S3 antibody (AA 1-202)
BLOC1S3
Reactivity: Human
IF, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-BLOC1S3 Antibody
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Target
See all BLOC1S3 Antibodies
BLOC1S3
(Biogenesis of Lysosomal Organelles Complex-1, Subunit 3 (BLOC1S3))
Binding Specificity
All epitopes for BLOC1S3 antibodies
AA 1-202
Reactivity
All reactivities for BLOC1S3 antibodies
Human
Host
All hosts for BLOC1S3 antibodies
Rabbit
Clonality
All clonalities for BLOC1S3 antibodies
Polyclonal
Conjugate
All conjugates for BLOC1S3 antibodies
This BLOC1S3 antibody is un-conjugated
Application
All applications for BLOC1S3 antibodies
Immunofluorescence (IF), Immunohistochemistry (IHC)
Purpose
BLOC1S3 Rabbit pAb
Sequence
MASQGRRRRP LRRPETVVPG EATETDSERS ASSSEEEELY LGPSGPTRGR PTGLRVAGEA AETDSEPEPE PEPTAAPRDL PPLVVQRESA EEAWGTEEAP APAPARSLLQ LRLAESQARL DHDVAAAVSG VYRRAGRDVA ALASRLAAAQ AAGLAAAHSV RLARGDLCAL AERLDIVAGC RLLPDIRGVP GTEPEKDPGP RA
Cross-Reactivity
Human, Mouse, Rat
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-202 of human BLOC1S3 (NP_997715.1).
Isotype
IgG
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Discover our top product BLOC1S3 Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC,1:50 - 1:200,IF,1:50 - 1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for BLOC1S3
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Target
BLOC1S3
(Biogenesis of Lysosomal Organelles Complex-1, Subunit 3 (BLOC1S3))
Alternative Name
BLOC1S3 (BLOC1S3 Products )
Background
This gene encodes a protein that is a component of the BLOC1 multi-subunit protein complex. This complex is necessary for the biogenesis of specialized organelles of the endosomal-lysosomal system, including platelet dense granules and melanosomes. Mutations in this gene cause Hermansky-Pudlak syndrome 8, a disease characterized by lysosomal storage defects, bleeding due to platelet storage pool deficiency, and oculocutaneous albinism.,BLOC1S3,BLOS3,HPS8,RP,Signal Transduction,BLOC1S3
Gene ID
388552
UniProt
Q6QNY0
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