Home > Product > Antibody > Rabbit Anti-ATP6V1B2/FITC Conjugated antibody
V-ATPase B2; ATP6B1B2; ATP6B2; ATP6V1 B2; ATP6V1B 2; ATP6V1B2; ATPase H+ transporting lysosomal 56/58kDa V1 subunit B isoform 2; ATPase H+ transporting lysosomal 56/58kDa V1 subunit B2; ATPase H+ transporting, lysosomal (vacuolar proton pump) beta polypep
Cat:
SL12549R-FITC
Species Reactivity:
(predicted: Human,Mouse,Rat,Chicken,Dog,Pig,Cow,Horse,Rabbit,Sheep,Cynomolgus Monkey, Orangutan)
Immunogen:
KLH conjugated synthetic peptide derived from human ATP6V1B2
Format:
Lyophilized or Liquid
Storage instructions:
Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of ant
Buffer:
0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
ICC=1:50-200IF=1:50-200not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Calculated MW:
56kDa
More
Unit:
Price: $
Product PDFs
Datasheet:


background:
Vacuolar-type H+-ATPase (SLVATPase) is a multisubunit enzyme responsible for acidification of eukaryotic intracellular organelles. SLVATPases pump protons against an electrochemical gradient, while F-ATPases reverse the process, thereby synthesizing ATP. A peripheral V1 domain, which is responsible for ATP hydrolysis, and a integral V0 domain, which is responsible for proton translocation, compose SLVATPase. Nine subunits (A–H) make up the V1 domain and five subunits (a, d, c, c' and c") make up the V0 domain. Like F-ATPase, SLVATPase most likely operates through a rotary mechanism. The SLVATPase V1 B subunit exists as two isoforms. In the inner ear, the SLVATPase B1 isoform functions in proton secretion and is required to maintain proper endolymph pH and normal auditory function. The gene encoding the human SLVATPase B1 isoform maps to chromosome 2cen-q13. Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness. The SLVATPase B2 isoform is expressed in kidney and is the only B isoform expressed in osteoclasts. The gene encoding the human SLVATPase B2 isoform maps to chromosome 8p22-p21.

Function:
Non-catalytic subunit of the peripheral V1 complex of vacuolar ATPase. SLVATPase is responsible for acidifying a variety of intracellular compartments in eukaryotic cells.

Subunit:
SLVATPase is a heteromultimeric enzyme composed of a peripheral catalytic V1 complex (main components: subunits A, B, C, D, E, and F) attached to an integral membrane V0 proton pore complex (main component: the proteolipid protein).

Subcellular Location:
Endomembrane system. Melanosome. Endomembrane. Identified by mass spectrometry in melanosome fractions from stage I to stage IV.

Similarity:
Belongs to the ATPase alpha/beta chains family.

Database links:

Entrez Gene: 526 Human

Entrez Gene: 11966 Mouse

Entrez Gene: 100173673 Orangutan

Entrez Gene: 117596 Rat

Entrez Gene: 338082 Cow

Omim: 606939 Human

SwissProt: P31408 Cow

SwissProt: P21281 Human

SwissProt: P62814 Mouse

SwissProt: Q5R5V5 Orangutan

SwissProt: P62815 Rat

Unigene: 295917 Human

Unigene: 249096 Mouse

Unigene: 8109 Rat



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Product Feedback Wall
Message :
Your Email :
Copyright © 2007-2018 Sunlong Medical All Rights Reserved.